“uniquely in this Circuit, the Daubert factors have been employed also as an acceptable evidentiary-gauging tool with respect to persuasiveness of expert testimony already admitted”
How later courts described this case
- “uniquely in this Circuit, the Daubert factors have been employed also as an acceptable evidentiary-gauging tool with respect to persuasiveness of expert testimony already admitted”
- “[i]t has generally been held that oral testimony which is in conflict with contemporaneous documents is entitled to little evidentiary weight.”
- “medical records and medical opinion testimony are favored in vaccine cases, as treating physicians are likely to be in the best position to determine whether a ‘logical sequence of cause-and-effect show[s] that the vaccination was the reason for the injury’”
- “like any norm based upon common sense and experience, this rule should not be treated as an absolute and must yield where the factual predicates for its application are weak or lacking”
Written by the judges who cited it.
The opinion
In the United States Court of Federal Claims
OFFICE OF SPECIAL MASTERS
No. 15-792V
Filed: April 15, 2022
************************* *
*
HEATHE HELLER and JENNA HELLER, **
parents of H.H., a minor, * TO BE PUBLISHED
*
Petitioners, * Aicardi–Goutières syndrome (AGS);
*
* Type I Interferonopathy; Pentacel
v. * vaccine; influenza vaccine; Prevnar
* vaccine; insufficient proof of causation
SECRETARY OF HEALTH AND *
HUMAN SERVICES, *
*
*
Respondent. *
*
************************* *
Margaret Guerra, Margaret M. Guerra, Attorney at Law, Fort Worth, TX, for Petitioners
Adriana Teitel, U.S. Department of Justice, Washington, DC, for Respondent
DECISION ON ENTITLEMENT1
Oler, Special Master:
On July 27, 2015, Heathe Heller (“Mr. Heller”) and Jenna Heller (“Mrs. Heller”)
(collectively “Petitioners”) filed a petition for compensation under the National Vaccine Injury
Compensation Program, 42 U.S.C. § 300aa-10, et seq.2 (the “Vaccine Act” or “Program”) alleging,
1
This Decision will be posted on the United States Court of Federal Claims’ website, in accordance with
the E-Government Act of 2002, 44 U.S.C. § 3501 (2012). This means the Decision will be available to
anyone with access to the internet. As provided in 42 U.S.C. § 300aa-12(d)(4)(B), however, the parties
may object to the Decision’s inclusion of certain kinds of confidential information. To do so, each party
may, within 14 days, request redaction “of any information furnished by that party: (1) that is a trade secret
or commercial or financial in substance and is privileged or confidential; or (2) that includes medical files
or similar files, the disclosure of which would constitute a clearly unwarranted invasion of privacy.”
Vaccine Rule 18(b). Otherwise, this Decision will be available to the public in its present form. Id.
2
National Childhood Vaccine Injury Act of 1986, Pub. L. No. 99-660, 100 Stat. 3755. Hereinafter, for ease
of citation, all “§” references to the Vaccine Act will be to the pertinent subparagraph of 42 U.S.C. § 300aa
(2012).
1
in part, that as a result of his October 17, 2013 vaccinations with influenza and Prevnar3 and his
October 23, 2013 vaccination with Pentacel,4 H.H. experienced either the onset or the significant
aggravation of his degenerative neurologic disorder.
For the reasons discussed in this decision, I find that H.H.’s vaccinations did not cause or
significantly aggravate his condition.
I. Procedural History
On July 27, 2015, Heathe and Jenna Heller, on behalf of their minor son, H.H. filed a
petition5 seeking compensation under the Vaccine Act, alleging that H.H. suffered from dystonia
and encephalopathy as a result of the influenza (“flu”) and Prevnar vaccines he received on
October 17, 2013, and/or the DTaP-IPV-Hib (Pentacel) vaccination he received on October 23,
2013. Pet. at 1.
Petitioners filed medical records on August 3, 2015. ECF No. 10. Petitioners filed
additional medical records, affidavits, and expert reports from Dr. Leslie Hollis and Dr. Warren
Marks on October 9, 2015. ECF No. 14. Petitioner filed additional medical records on November
9, 2015 (ECF No. 16) as well as a statement of completion on November 9, 2015 (ECF No. 17).
On February 1, 2016, Respondent filed his Rule 4(c) Report, asserting that the case was
not appropriate for compensation and should be dismissed. Resp’t’s Rep. ECF No. 21.
Petitioners filed additional affidavits and exhibits on March 21, 2016. ECF No. 28.
Petitioner also submitted a supplemental expert report from Dr. Hollis on the same date. Id.
On July 8, 2016, Special Master Hastings held a status conference. ECF No. 35. Special
Master Hastings stated to Petitioners’ counsel that “as this case proceeds, it is imperative that all
the evidence is identified in a manner that does not cause confusion.” See Scheduling Order of
July 8, 2016, ECF No. 35 at 1. Accordingly, Special Master Hastings ordered Petitioners to re-
number and re-file all of Petitioner’s exhibits that had been filed previously. Id. Special Master
Hastings noted that “the numbering of these re-filed exhibits shall commence with exhibit number
48, followed by consecutive exhibits numbers thereafter.” Id.
Accordingly, Petitioners refiled all previously submitted medical records, affidavits, and
expert reports on August 26, 2016. Exs. 48-93, ECF Nos. 40-46.
3
Prevnar is a “trademark for a preparation of pneumococcal 7-valent conjugate vaccine.” Prevnar,
Dorland’s Med. Dictionary Online, https://www.dorlandsonline.com/dorland/definition?id=40909&
searchterm=Prevnar (last accessed April 13, 2022).
4
Pentacel is a “trademark for a combination preparation of diphtheria and tetanus toxoids and acellular
pertussis vaccine adsorbed, poliovirus vaccine inactivated, and Haemophilus b conjugate (tetanus toxoid
conjugate) vaccine.” Dorland’s Med. Dictionary Online, Pentacel, https://www.dorlandsonline.com/
dorland/definition?id=37544&searchterm=Pentacel (last accessed April 13, 2022).
5
Petitioners filed an amended Petition on November 9, 2015. ECF No. 15.
2
On December 14, 2016, Respondent filed an expert report from Dr. Kristin Barañano. Ex.
A, ECF No. 52. Respondent filed Dr. Barañano’s CV at Exhibit B. On the same date, Respondent
filed the medical literature associated with Dr. Barañano’s report. Exs. A-1 – A-5, ECF No. 52.
On August 25, 2017, Petitioners filed a supplemental expert report from Dr. Warren Marks.
Ex. 94, ECF No. 54.
This case was reassigned to my docket on December 5, 2017. ECF No. 59. Petitioners filed
additional medical records on March 6, 2018. Ex. 95, ECF No. 61.
On August 17, 2018, Respondent filed a supplemental expert report from Dr. Barañano.
Ex. C, ECF No. 67. Respondent filed the medical literature associated with Dr. Barañano’s report
as Exhibit C-1 on the same date.
On April 29, 2019, Respondent filed an expert report from Dr. Stephen McGeady. Ex. D,
ECF No. 70. Respondent filed Dr. McGeady’s CV at Exhibit E.6 Respondent filed the medical
literature associated with Dr. McGeady’s report on the same day. Exs. D-1 – D-12, ECF No. 71.
On December 31, 2019, the parties filed their pre-hearing submissions. ECF Nos. 75-76.
Pre-hearing briefs were filed on January 8, 2020. ECF Nos. 78-79.
On January 8, 2020, Respondent filed two additional pieces of medical literature. Exs. F,
G, ECF No. 81.
I held an entitlement hearing on January 22, 2020. ECF No. 88. At the conclusion of the
hearing, I held a status conference with the parties during which several items were discussed. See
Scheduling Order of January 29, 2020, ECF No. 86. I directed Petitioners’ counsel to file several
documents, including:
1. Any emails and/or records from Dr. Yanick Crow, including the results of the genetic
testing done by Dr. Crow.
2. Any medical records from the Panama clinic where H.H. underwent multiple stem cell
treatments as referenced in Ex. 96, pg. 36.
3. Medical records from H.H’s Boston Children’s Hospital visit.
4. Medical records and/or genetic testing results from Atlanta.
5. Any additional photos or videos of H.H. from Halloween 2013.
6. A status report identifying the specific dates of the video clips in Ex. 47.
7. Additional medical records from H.H.’s most recent visits with Dr. Warren Marks.
8. A status report informing the Court as to whether Petitioners wished to file additional
expert reports.7
6
Respondent re-filed Dr. McGeady’s CV on April 14, 2020. Ex. I, ECF No. 90.
3
Id. at 1-2. In addition, Respondent was ordered to file an updated CV for Dr. Barañano and Dr.
McGeady, and the parties were ordered to file medical literature summaries by March 31, 2020. 8
Id. at 2.
Petitioners filed a status report on April 14, 2020, stating that they had employed Dr.
Lawrence Steinman to provide an additional expert report. Petitioners’ Status Report of April 14,
2020, ECF No. 92. Petitioners stated that they had only been able to retrieve some of the medical
records that were requested in my January 29, 2020 order, and filed these on the same day. Exs.
97-100, ECF No. 93.
On July 24, 2020, Petitioners filed an expert report from Dr. Steinman. Ex. 101, ECF No.
95. Petitioners filed the medical literature associated with Dr. Steinman’s report on the same date.
Exs. 101-1 – 101-20, ECF No. 101.
On December 1, 2020, Respondent filed a rebuttal expert report from Dr. McGeady. Ex. J,
ECF No. 104.
On February 12, 2021, Petitioners filed a supplemental expert report from Dr. Steinman.
Ex. 99, ECF No. 108 (hereinafter “Second Steinman Rep.”).
9
On May 15, 2021, Petitioners filed their post-hearing brief. ECF No. 113. Respondent filed
a response on July 8, 2021. ECF No. 116. Petitioners filed a reply on July 15, 2021. ECF No. 118.
On August 9, 2021, the parties filed a joint status report indicating that the record was
complete. ECF No. 119.
On March 15, 2022, my law clerk emailed the parties in order to inform Petitioners’ counsel
that one exhibit referenced during the hearing (a letter from Sheri Huling to Petitioners’ counsel
which served as the basis for Ms. Huling’s affidavit) had not been filed into the record. That same
day, I entered an order directing Petitioners to file the letter as soon as practicable See Non-PDF
Informational Communication of March 15, 2022. Petitioners filed on the letter on March 23,
2022. Ex. 102; ECF No. 120.
This matter is now ripe for adjudication.
7
At the conclusion of the entitlement hearing after we went off the record, I informed Petitioners’ counsel
that the record, as it currently stood, did not enable Petitioners to meet their burden. I suggested that
Petitioners’ counsel consider retaining an additional expert neurologist so that Petitioners may be afforded
a full and fair opportunity to prosecute their case.
8
This additional documentation filed on April 14, 2020. ECF No. 90.
9
Petitioners inadvertently labeled this report as Exhibit 99. Exhibit 99 is already a medical record. To avoid
confusion, I have referred to this report as “Second Steinman Rep.” in this decision.
4
II. Medical Records
A. Relevant Pre-Vaccination History
H.H. was born on July 14, 2012. Ex. 48 at 1. H.H. was delivered vaginally with no
complications. Ex. 49 at 5.
On July 18, 2012, H.H. was seen by Dr. Leslie Hollis at Wise Pediatrics for a newborn
visit. Ex. 49 at 5. H.H. was noted as meeting all his newborn milestones: raising his head when
prone, making eye contact/regarding faces, startling to noise, following to midline and equal
movements. Id. H.H. was sleeping three to four hours at a time, and his parents indicated no
concerns at this visit. Id. Dr. Hollis noted no abnormalities. Id. at 5-6. H.H. was scheduled to return
in one week for a weight check. Id. at 6.
On July 23, 2012, H.H. visited Dr. Hollis at Wise Pediatrics to follow up on an abnormal
newborn screen “possibly indicating a VLCAD deficiency.”10 Ex. 49 at 7. Dr. Hollis noted that
H.H. “has been doing very well. Weight gain and breastfeeding going well.” Id. H.H. was observed
as “playful, alert and aware” and Dr. Hollis found no abnormalities upon examination. Id. Dr.
Hollis ordered a Texas newborn screen, a plasma acylcarnitine profile, and a urine organic acids
test. Id.
On July 27, 2012, H.H. visited Dr. Hollis at Wise Pediatrics for a two-week well child visit.
Ex. 49 at 9. His parents had no concerns at this visit. Id. Dr. Hollis observed no abnormalities upon
examination. Id. H.H.’s Texas Newborn Screen was canceled at this visit. Id. at 10. H.H. was next
scheduled to return for his two-month wellness check.
On August 1, 2012, RN Michelle Johns from Wise Pediatrics left a voicemail for Mrs.
Heller, indicating that H.H.’s second PKU (Phenylketonuria) screening was normal. Ex. 49 at 11.
On August 8, 2012, LVN Cozby called Mrs. Heller to inform her that the rest of H.H.’s
labs returned normal results. Ex. 49 at 14.
On August 16, 2012, RN Johns called Mrs. Heller and left her a voicemail informing her
that “State is requiring a referral to Dr. Basinger[, a] metabolic geneticist since [H.H.’s] first [PKU
screening] was abnormal.” Ex. 49 at 15. Petitioner called back the same day to confirm an
appointment with Dr. Basinger. Id. at 16.
On August 23, 2012, Dr. Heather Crawford sent a letter to Dr. Hollis noting that H.H was
under evaluation for a VLCAD deficiency, which could cause hypoglycemia, cardiomyopathy,
elevated ammonia levels, abnormal liver function tests, and death should H.H. have prolonged
10
A VLCAD deficiency “is a condition in which the body is unable to properly breakdown certain fats
(called very long-chain fatty acids) into energy, particularly during periods without food (fasting).” National
Institutes of Health, National Center for Advancing Translational Sciences, VLCAD Deficiency, https://
rarediseases.info.nih.gov/diseases/5508/vlcad-deficiency#:~:text=VLCAD%20deficiency%20is%20a%20
condition,periods%20without%20food%20(fasting) (last accessed April 8, 2022).
5
fasting or poor dietary intake due to illness. Ex. 89 at 14. She noted that H.H.’s blood glucose
needed to be maintained at about 70 mg/dL. Id.
On September 18, 2012, H.H. visited Dr. Hollis at Wise Pediatrics for his two-month well-
child visit. Ex. 49 at 18. H.H.’s parents had no concerns at this visit. Id. H.H. was recorded as
meeting all his developmental milestones: grasping a rattle, presenting a social smile, cooing,
responding to a bell, following past midline, and parent/child interaction. Id. H.H. weight 11.7
pounds. Id. Dr. Hollis noted no abnormalities upon examination. Id. at 18-19. H.H. received his
Prevnar-13, Hepatitis B, Pentacel, and Rotarix vaccines at this visit. Id. at 19. H.H. was next
scheduled to be seen for his four-month well child appointment. Id.
On November 14, 2012, H.H. was seen by Dr. Hollis at Wise Pediatrics for his four-month
well child visit. Ex. 49 at 21. H.H. was noted to be sleeping “more than 10 hours per night”. Id.
His parents voiced no concerns at this visit. Id. H.H. was noted to be meeting all his developmental
milestones: raising his body on his hands, steady head control when held upright, no head lag when
pulling to sit, rolling “prone to supine”, grasping his rattle, playing with his hands/bringing his
hands together, turning to sound, following objects 180 degrees, and laughing/squealing. Id. H.H.
weighed 14.06 pounds. Id. Dr. Hollis observed no abnormalities upon examination. Id. at 22. H.H.
received his Prevnar-13, Pentacel, and Rotateq vaccinations at this visit. Id. H.H. was next
scheduled to return for his six-month well child visit. Id.
On January 23, 2013, H.H. was seen by Dr. Hollis at Wise Pediatrics for his six-month
well visit. Ex. 49 at 26. H.H. was noted to be meeting all his developmental milestones: rolling
over both ways, sitting with minimal support, no head lag when pulling to sit, bearing weight,
transferring objects from hand to hand, laughing/babbling and imitating sounds, turning towards
voices, “raking raisin”, looking “for yarn” and reaching for objects/working for toys. Id. at 27.
H.H. weight 16.87 pounds at this visit. Id. Dr. Hollis noted no abnormalities upon examination.
Id. at 27-28. H.H. received his Prevnar-13, HiB, Pediarix, Rotateq, and flu vaccinations at this
appointment. Id. at 28. Dr. Hollis noted that H.H. had “no problems with previous immunizations.”
Id. H.H. was next scheduled to be seen for his nine-month well child visit. Id.
On April 16, 2013, H.H. visited Dr. Hollis at Wise Pediatrics for his nine-month well visit.
Ex. 49 at 28. By this point, H.H. had begun eating solid foods, including fruits, Cheerios, and
yogurt. Id. He was sleeping more than ten hours per night and his parents had no concerns. Id.
H.H. was noted to be meeting all his developmental milestones: Sitting well, crawling, pulling to
stand and cruising, using a pincer grasp, banging two toys together, finger feeding, babbling
mama/dada, playing peek-a-boo, indicating his wants, and waving bye-bye. Id. Dr. Hollis noted
no abnormalities upon examination. Id. at 28-29. H.H. weighed 18.77 pounds at this visit. Id. at
29. H.H. was next scheduled to be seen for his 12-month well child visit. Id.
On July 18, 2013, H.H. was seen by Dr. Hollis at Wise Pediatrics for his 12-month well
child visit. Ex. 49 at 33. By this time, H.H. had switched to whole milk from formula, was eating
solids to include meats and Gerber Graduates, and was sleeping more than ten hours per night. Id.
His parents had no concerns at this visit. Id. H.H. was noted to be meeting all his developmental
milestones: pulling to stand/standing alone for 2-3 seconds, walking with support and taking a few
steps, precise pincer grasp, had a 1–3-word vocabulary, using Mama/Dada specifically, drinking
6
from a cup, understanding “no” and imitating actions. Id. H.H. weighed 21.34 pounds at this visit.
Dr. Hollis noted no abnormalities upon examination. Id. at 33-34. H.H. received his MMRV and
Hepatitis A vaccinations at this visit. Id. at 34. H.H. was next scheduled to be seen for his 15-
month well child visit. Id.
On July 29, 2013, H.H. was seen by Dr. Hollis at Wise Pediatrics for a sick child visit. Ex.
49 at 36. Under HPI, Dr. Hollis stated that “Pt has been running fever to 102 for the [past] 3 days.
Mom is also sick. He has had nasal congestion for 2 weeks.” Id. H.H. was diagnosed with purulent
rhinitis and prescribed Augmentin. Id.
On September 13, 2013, Petitioner called Wise Pediatrics and stated that she was concerned
with H.H. “not walking and right foot turned inward.” Ex. 49 at 37. LVN Cozby noted that H.H.
was scheduled for an appointment in one month and advised Petitioner, per Dr. Hollis, to wait until
that appointment to be seen. Id.
B. Post-Vaccination History
On October 17, 2013, H.H. visited Dr. Hollis at Wise Pediatrics for his 15-month well visit.
Ex. 49 at 1. At this visit, H.H. was noted as meeting all of his developmental milestones: Walking
alone, crawling up stairs, self-feeding with fingers, using a fork and spoon, talking with a three to
six word vocabulary, understanding simple commands, rolling/tossing a ball, stooping to recover
a toy, and indicating his wants without crying. Id. Upon physical exam, Dr. Hollis noted no
abnormalities. Id. H.H. received his influenza and Prevnar-13 vaccines at this appointment,
although he did not receive Pentacel.11 Id. Dr. Hollis discussed H.H.’s development, growth and
nutrition with Petitioner. Id. at 2. H.H. was next scheduled to return for his 18-month well child
visit. Id. at 2.
On October 23, 2013, H.H. was seen by Nurse practitioner Ariane Segura. Ex. 49 at 3. H.H.
received his Pentacel vaccination at this visit. Id.
On November 11, 2013, H.H. visited Dr. Hollis at Wise Pediatrics for a sick child visit.
Ex. 49 at 41. In the HPI, Dr. Hollis stated “Pt has been fussy for the last week. He has run fever to
101.5. His energy level is decreased. Pts development has regressed in the last month. He has
stopped crawl[]ing. He is not wanting to play with toys. He will throw toys and food.” Id. H.H.
was noted to be “playful, alert and aware” and in no respiratory distress. Id. Dr. Hollis observed
no abnormalities until she conducted a neurologic examination. She noted that H.H.’s reflexes
were “Brisk, 3+” and his tone was “hypotonic”. Id. A rapid strep throat test was negative and a
CBC returned normal results. Id. at 41-42. H.H. was diagnosed with a developmental delay and
acute pharyngitis. Id. at 42. He was referred to neurology “ASAP” for evaluation. Id. Petitioner
was instructed to try throat lozenges, fluids, and rest to treat the pharyngitis. Id.
On November 12, 2013, H.H. visited Dr. Heather Crawford at Cook Children’s Hospital,
Department of Clinical and Metabolic Genetics, for “new problem of loss of milestones, elevated
11
Mrs. Heller testified at the entitlement hearing that Wise Pediatrics was out of the Pentacel vaccine, and
she was told to return to get that vaccine at a later date. Tr. at 17.
7
liver enzymes.” Ex. 50 at 1. H.H. was observed to be “healthy-appearing, well-nourished, and
well-developed” and in no distress. Id. He was “active and alert and [with a] normal mood.” Id.
Upon examination, no abnormalities were found in an examination of his head, eyes, ears, nose,
throat, neck, chest, heart, abdomen, back, skin, hair and genitals. Id. at 1-2. Upon an examination
of H.H.’s musculoskeletal systems, Dr. Crawford noted that H.H. had “normal strength and
hypertonicity (noted in lower extremities especially at the ankles). Id. at 2. She stated that “his heel
cords appear somewhat tight and he may require AFOs at some point in the future.” Id. A
neurologic exam revealed that H.H. was “not walking yet” and was “not speaking yet.” Id. Dr.
Crawford also noted that H.H. had “elevated transaminases” but she “would like to repeat those
[tests] once his minor illness has passed.” H.H. was diagnosed as “a 16 month old who now
presents with a new history of developmental delay with loss of some developmental milestones.”
Id. Dr. Crawford ordered a “baseline genetic and metabolic workup to include looking for
chromosomal abnormalities and disorders of fat and protein metabolism.” Id. Additionally, she
ordered an “MRI of the brain to make sure that the gross anatomy of the brain is normal.” Id. She
recommended that Petitioners start H.H. in physical and speech therapy while the cause of his
developmental delay was diagnosed. Id. Concerning his “elevated transaminases”, Dr. Crawford
stated that if they were still elevated in a month, she would “expand our evaluation to include an
abdominal ultrasound to evaluate the liver and possible evaluate for lysosomal disorders if his
regression persists.” Id.
On November 14, 2013, Dr. Crawford sent a note to Dr. Hollis, providing the details of
H.H.’s visit on November 12, 2013. Ex. 50 at 4. Dr. Crawford stated that:
H.H. is a 16 month old male who is being referred again for an evaluation for
developmental delay and possible regression of milestones. He was initially seen
in the metabolic genetics clinic after an abnormal newborn screen for possible
VLCAD deficiency. However, follow up testing including a skin biopsy to look at
fat metabolism proved to be negative. He was then cleared for that screening test
with no follow up recommended at that time. However, I was contacted by his PCP,
Dr. Hollis, who was concerned about his development. She stated that he was sitting
at 6 months, crawling at 7 months and took a few steps at 10 months. He apparently
had 3 words at 12 months. Parents now state that he does not take any steps [] nor
does he pull to stand anymore. He now has no words. They also feel that his affect
is not normal in that he does not laugh spontaneously or much at all. He has been
sick with a virus this last couple weeks. He has not had any major illnesses or
hospitalizations since birth.
Id. Dr. Crawford’s notes indicate that H.H. was diagnosed with a developmental delay, specifically
a slight delay in gross motor function and fine motor function/ADLs, and a significant delay in
language functioning. Id.
On the same date, H.H. was admitted to the hospital with worsening symptoms. Ex. 51 at
5. Dr. Michael Aalbers, a neurologist, admitted H.H. to the hospital with “progressive dysarthria,12
12
Dysarthria is “a speech disorder consisting of imperfect articulation due to loss of muscular control after
damage to the central or peripheral nervous system.” Dysarthria, Dorland’s Med. Dictionary Online, https://
8
trouble swallowing, and a fairly dramatic spastic diplegia in the lower extremities.” Id. at 8. A CT
scan demonstrated “mild volume loss with no evidence of upper motor neuron injury.” Id. Dr.
Aalbers also noted that there was “no evidence of bony malformation, [or] concerns for acute
transverse myelitis.” Id. It was noted that H.H. was constipated but had “appropriate bowel and
bladder symptoms.” Id.
After being admitted, H.H. underwent a lumbar puncture to “rule out demyelinating disease
versus metabolic etiologies versus dopa-responsive dystonia.” Ex. 52 at 5. The lumbar puncture
revealed no significant results.
On November 15, 2013, H.H. underwent a brain MRI. Ex. 51 at 1. The clinical indication
was “acute onset spastic diplegia.” Id. Dr. Hayden Head interpreted the MRI. His impression was
“Mild enlargement of subarachnoid spaces. If the head circumference is enlarged and/or has been
rapidly increasing, the findings would be in keeping with benign enlargement of subarachnoid
spaces of infancy, in the appropriate clinical setting. If not, mild diffuse parenchymal volume loss
should be considered.” Id. Dr. Head noted that H.H.’s MRI was “otherwise unremarkable.”
On November 16, 2013, H.H. was discharged from the hospital. His discharge summary
stated:
[H.H.] presented to the emergency department and upon evaluation by Dr. Aalbers
of neurology was found to have significant dystonic posturing of the lower
extremities, prompting his admission. He was admitted to the floor in stable status.
The workup included an MRI of the brain, which was within normal limits. An
MRI of the complete spine was significant only for a fatty film, suggesting a
possible tethered cord.
Ex. 51 at 5. Dr. Michael Perry, H.H.’s discharging physician, stated that “during admission,
[H.H.’s] irritability decreased significantly, and he was able to feed fairly well.” Id. H.H. was
treated with Sinemet for “presumptive dopa-responsive dystonia” and seemed to respond to the
treatment. Id. Dr. Perry noted that confirmation of diagnoses would depend on CSF results. Id.
H.H.’s family was instructed to call the hospital if H.H. had increased irritability, increased tone,
intolerance to medication, or any other concerns. Id. at 6.
On November 21, 2013, Dr. Elisabeth Brockie, DO, of Quest Diagnostics – Dallas
provided lab results for H.H.’s lactate and plasma acylcarnitine. Ex. 50 at 54. She noted that
“several very-long-chain and long-chain-hydroxy acylcarnitine species were minimally to mildly
elevated” in the sample she tested. Id. She noted that the results were “not sufficient” to rule out a
mitochondrial fatty acid disorder. Id. She noted that these results have been seen in “liver disease,
some mitochondrial disorders, metabolic stress, certain glycogen storage disorders, and
generalized sickness of not metabolic origin.” Id. An amino acids lab result reported on the same
day showed “elevated” amino acids but did “not suggest a specific inherited metabolic disorder.”
Id. at 56.
www.dorlandsonline.com/dorland/definition?id=15144&searchterm=dysarthria (last accessed April 8,
2022).
9
On November 22, 2013, H.H. was seen by Dr. Aalbers at Cook Children’s Hospital. Ex.
52 at 8. Problems reviewed included “cough, spinal cord disease, dystonia, screening finding,
speech delay and delayed milestone.” Id. In the patient history, Dr. Aalbers noted that H.H. was at
the clinic “emergently secondary to concerns of rapidly advancing metabolic neurodegenerative
disease” and that since his discharge from the hospital on November 16, 2013, H.H. had
progressively lost meaningful use of his right hand. Id. at 9. Upon examination, Dr. Aalbers found
no abnormalities in H.H.’s eyes, ears, nose, mouth, throat, heart, respiratory systems,
gastrointestinal symptoms, musculoskeletal systems, or skin. Upon conducting a neurologic
examination, Dr. Aalbers noted that H.H. had “weakness, trouble walking, and poor attention.” Id.
at 10. H.H.’s mental status was described as “somnolent.” Id. His grasp of language was considered
“dysfluent and dysarthric” and his “fund of knowledge” was “delayed for age. Id. During a motor
exam, Dr. Aalbers observed the following:
Motor spastic, rigidity, hypotonic axial, hypertonia appendicular, and dystonia
diffuse and normal bulk and no focal weakness; Patient has internal rotation and
supination with dystonic posturing of the thumb in the right hand that was not
present 4 days ago with intermittent scissoring of the lower extremities dystonic
spastic posturing of the feet with plantarflexion striatal toes bilaterally patient has
appropriate head[] control with increased tone and cogwheeling on the right but
good range of motion of his fingers.
Id. at 10. Finally, in examining H.H.’s spine, Dr. Aalbers observed “no tenderness and decreased
ROM” in H.H.’s cervical spine. Id. Dr. Aalbers’ initial impression was “rapidly progressive
ascending dystonia with encephalopathy – Concern for mitochondrial disease versus lysosomal
storage disease/inborn error of metabolism.” Id. at 11. Dr. Aalbers also provided his impression of
H.H.’s testing from his hospital stay (November 14, 2013 – November 16, 2013):
In the interim the patient was admitted to the hospital with subsequent concerns for
rapidly progressive dysarthria choking with exacerbation dystonic posturing in the
lower extremities. Patient matter and lumbar puncture which demonstrated no
evidence of pleocytosis with normal lactate pyruvate urine organic acids and repeat
[] acylcarnitine profile.
Subsequent neuroimaging demonstrates numerous white matter hyperintensities
particularly along the insula bilaterally however this is still within the normal range
of normal myelination for [a] 16- month-old, there is perhaps mild volume loss in
the midline particularly midline stratum without signal change.
MRI of his lower spine demonstrates a mildly tethered cord that would not explain
the dystonia or striatal toe [but] may explain the constipation rapid exag[g]eration
of symptoms.
Id. at 11. Dr. Aalbers noted that “within a week [of his discharge, H.H. developed] increased
encephalopathy and now has los[t] meaningful[] use of his right hand with cogwheeling of his left
despite being on 25 100 mg of Sinemet secondary to a working diagnosis of rapidly progressive
10
to responsive dystonia.” Id. A metabolic geneticist did not suspect that H.H. had a “fatty acids
oxidation disorder based on the fibroblast and repeated carnitine profiles” and an EEG
demonstrated “no evidence of epilep[t]iform [discharges].” Id. Dr. Aalbers’ differential diagnosis
was “rapidly progressive primary mitochondrial disease.” Id. Dr. Aalbers stated that he would
order testing for lysosomal storage diseases, and “full scale mitochondrial studies.” Id. H.H.’s
parents were instructed to continue Sinemet 25 100 and observe H.H. for worsening
encephalopathy or new symptoms. Id.
That same date, H.H. underwent an EEG. Ex. 52 at 47. Dr. Howard Kelfer, interpreting the
EEG, stated that “this tracing, recorded while awake and during sleep, is mildly abnormal. The
background activity is somewhat slow for age. The findings are indicative of a mild to moderate
diffuse disturbance of brain function. There is no definite epileptiform activity.” Id.
On November 23, 2013, Dr. Thomas Lohmann provided the results of H.H.’s genetic
testing conducted using a microarray analysis, stating that “no deletions or duplications of known
or potential clinical significance were detected by microarray analysis.” Ex. 50 at 61.
On November 27, 2013, Medical Neurogenetics Laboratories (“MNG Labs”) provided the
results of the testing ordered by Dr. Aalbers. Ex. 52 at 19. Under “neurotransmitter metabolics”,
H.H.’s 5-Hydroxindoleacetic acid was slightly elevated, with a value of 215 mnol/L (reference
range 67-189 nmol/L). Id. Dr. Keith Hyland, Ph.D, interpreting the results stated that “this is
unlikely to be of any clinical significance.” Id. at 20. Under “tetrahydrobiopterin and neopterin
profile”, H.H.’s neopterin was extremely elevated, with a value greater than 300 nmol/L (reference
range 8-33 nmol/L). Id. H.H.’s tetrahydrobiopterin was also extremely elevated at 118 nmol/L
(reference range 9-33 nmol/L). Dr. Hyland noted that “elevations of neopterin and
tetrahydrobiopterin have been described in the Aicardi-Goutieres syndrome” and “we have also
noted a similar abnormal pterin pattern in HIV infection.” Id. All other testing was normal. Id. at
19-20, 23.
On December 3, 2013, H.H. was seen by Dr. Aalbers for “neurological regression.” Ex. 52
at 25. Dr. Aalbers noted generally the same problems he had observed during H.H.’s November
22, 2013 visit. Id. at 25-26. Under “Impression”, Dr. Aalbers stated that H.H.’s diagnosis was
“rapidly progressive dystonia and encephalopathy” with “concern for possible Accardi-Gutierres
[sic]”. Id. at 28. Dr. Aalbers stated that H.H had:
Rapidly progressive dystonia, now with lo[ss of] meaningful [use] of his left hand
and spastic dystonic scissoring of the lower extremities. In the interim [h]is
neurotransmitter results surprisingly showed marked elevation to biopterin in the
option which is commonly seen in patients with inflammatory encephalitis such as
[] AGS. Of concern the patient had previously unexplained transient elevations of
liver enzymes which is consistent with AGS as is progressive encephalopathy and
dystonia spasticity.
Id. at 28. Dr. Aalbers also noted that H.H.’s MRI was “confusing”, noting that “there are patchy
white matter hyperintensities throughout however given his chronological age patchy
hypomyelination can be normal.” Id.
11
To confirm the diagnosis, Dr. Aalbers arranged for HIV testing, repeat of H.H.’s
neurotransmitters studies, and planned to contact experts in AGS. Id. H.H. was referred to Dr.
Heather Crawford for additional genetic testing in connection with AGS. Id.
On December 3, 2013, H.H. was seen by Dr. Crawford at Cook Children’s Hospital,
Department of Clinical and Metabolic Genetics for a follow up evaluation for “developmental
regression with dystonia.” Ex. 50 at 11. No abnormalities were found upon an evaluation of H.H.’s
head, eyes, ears, nose, mouth throat, neck, genitals, back, skin, or hair. Id. at 11-12. A
musculoskeletal exam revealed that H.H. had “normal strength and hypertonicity (noted in lower
extremities especially at the ankles, feet held inward position); Pt now holds hand in a fist when
trying to reach for objects and when crawling, then afterward hand relaxes when trying to hold a
bottle.” Id. at 11. A neurologic exam revealed that H.H. was “not walking yet” and “not speaking
yet.” Id. H.H. was assessed as “a 16 month old who now presents with a new history of
developmental regression and onset of progressive dystonia in the last 2-3 months.” Id. at 12. He
was diagnosed with delayed milestones, unspecified encephalopathy, speech delay (“expressive
language disorder”), and dystonia (“unspecified extrapyramidal disease and abnormal movement
disorder”). Id.
In the discussion notes, Dr. Crawford stated:
[H.H.] continues to have dystonia in the lower extremities, however his hands are
now becoming involved. He is still unable to crawl or pull [to] stand. He is now
having difficulties sitting alone. His clinical picture is very concerning for either a
metabolic or neurogenetic disorder. He had CSF studies done that included
neurotransmitters which showed an extremely elevated neopterin and
tetrahydrobiopterin. The lab's interpretation stated that only Aicardi-Goutières
syndrome and HIV infection would cause such high values. Dr. Aalbers and myself
have discussed this case at length. He does not have the typical presentation of AGS
as he does not have any calcifications in the brain and did not present with
thrombocytopenia, hepatosplenomegaly with elevated liver enzymes after birth.
However, there are milder presentation[s] of this syndrome where the calcification
can develop after 1-2 year of age. Therefore, this disorder remains on our
differential. I got permission from the family to contact a Dr. Yanick Crow in
England who is a world expert on AGS to get his opinion.
Id. Dr. Crawford recommended that the lumbar puncture be repeated, as well as a test for IFN-
alpha in the CSF. Id. She stated that, aside from AGS, “mitochondrial disorders are still in the
differential as he has had an elevated lactate in the past, however repeat was normal.” Id. Dr.
Crawford ordered sequencing of H.H.’s mitochondrial genome and stated that “ [S]ince his
differential is still so wide at this point, we will proceed with whole exome sequencing which will
include the mitochondrial genome. This will also look at the 5 genes known to be associated with
Aicardi-Goutieres syndrome.” Id. Dr. Crawford encouraged “intensive therapies to help condition
his muscles and help with regaining milestones.” Finally, Dr. Crawford ordered additional
biochemical labs for diagnostic purposes. Id.
12
On December 4, 2013, Dr. Crawford sent a note to Dr. Hollis, providing the details of
H.H.’s visit on December 3, 2013. Ex. 50 at 14. Dr. Crawford stated that:
[H.H.] was last seen in the metabolic genetics clinic on 11/12/2013. At that time,
some metabolic labs were ordered as well as PT and ST. However, 2 days after our
clinic visit, parents felt that he was worsening. They felt he had difficulty
swallowing, increase[d] tone in his legs and increased irritability.
Id. Dr. Crawford noted that H.H. was admitted to the hospital on November 14, 2013 by Dr.
Aalbers in the neurology department. She stated that:
[Dr. Aalbers] felt that he had significant dystonic posturing of his lower extremities.
This led to an emergent MRI of the brain and a lumbar puncture for CSF studies.
He also had some other metabolic labs drawn during that admission. His irritability
improved and he was feeding well by time of discharge on Saturday 11/16/13. He
was started on sinemet during this admission due to the suspicion of dopa-
responsive dystonia. There was a slight improvement in his tone by discharge from
the hospital.
Id. Dr. Crawford further noted that:
Since discharge from the hospital, he continues to get physical therapy. Parents felt
that he was [sleepier] and the increased tone has returned to his legs. His hands
appear to be affected as the parents state that he does not use them as much as before
and he seems frustrated when trying to use his hands, but he is not able to open
them up to use them. Id.
Dr. Crawford noted that “[H.H.] was seen back in clinic by Dr. Aalbers on 11/22/13 and he felt
that his right hand was more dystonic.” Id. A swallow study conducted in the hospital returned
normal results, and an EEG did not demonstrate any seizure activity although “there was mildly
slow background activity.” Id. Dr. Crawford noted that “CSF neurotransmitter studies done on
11/14/13 returned and were abnormal. The neopterin and tetrahydrobiopterin were significantly
elevated.” Id. Lab testing revealed “several long chain acylcarnitine elevated right at the cutoff
ranges” and a “pattern of mildly elevated acids not in a pattern for specific disorder.” Id. at 15. A
brain MRI revealed “mild cerebral volume loss, myelination normal for his age.” Id. Dr.
Crawford’s notes again indicated that H.H. was diagnosed with a developmental delay, specifically
a slight delay in gross motor function and fine motor function/ADLs, and a significant delay in
language functioning. Id.
On December 9, 2013, H.H. underwent an EEG which returned normal findings. Ex. 52 at
45.
On December 18, 2013, H.H. was seen by Dr. Richard Roberts at Cook Children’s Hospital
Neuroscience Center for a consultation regarding his tethered spinal cord. Ex. 53 at 1. In the HPI,
Dr. Roberts noted that H.H. was a
13
16-month-old patient who was referred to neurosurgery for findings of a tethered
spinal cord on MRI. The patient was initially worked up for rapid onset of
developmental delay and hypertonia and a possible loss of motor skills. In the
course of workup the patient had [an] MRI which showed a thickened and fat
infiltrated filum terminale. The patient also suffers from constipation. Prior to the
rapid neurologic changes the patient also dragged his right foot.
Id. Dr. Roberts explained the benefits and risks of surgical release of tethered spinal cord to H.H.’s
parents, who indicated they wished to proceed with surgery. Id.
On December 19, 2013, H.H. underwent surgery to release his tethered spinal cord. Ex. 53
at 7. During surgery Dr. Roberts collected cerebrospinal fluid to be tested by neurology. Id. at 8.
Dr. Roberts noted that the procedure was successful and H.H. tolerated the procedure well. Id. He
was taken to recovery in stable condition. Id.
Following surgery, H.H. was seen by Dr. Aalbers. Ex. 55 at 1. Dr. Aalbers noted that the
lumbar puncture showed “remarkably high elevations of biopterin and neopterin; the highest
neopterin levels we have ever seen.” Id. Dr. Aalbers noted that the differential diagnosis in a patient
with new-onset dystonia and significantly elevated neopterin levels was likely “Aicardi-
[Goutières] syndrome.” Id. H.H.’s brain MRI was “completely normal”, but in the interim, he
continued to regress developmentally and was no longer using his arms. Id. Dr. Aalbers also wrote
that H.H.’s elevations of his liver enzymes (325 for the AST and 472 for the ALT) were also
indicative of possible AGS. Id. He noted that H.H. had been “intermittently lethargic, tired more
so than usual over the last 3 or 4 months without significant weight gain.” Id. at 2.
Dr. Aalbers laid out next steps for H.H.’s treatment. Ex. 55 at 3. He ordered an ultrasound
of H.H.’s liver and spleen, noting that “fluctuating liver inflammation and spleen inflammation
can be consistent with Aicardi-Goutieres syndrome with subsequent resolution of the syndrome.”
Id. at 3-4. Dr. Aalbers also ordered a repeat EEG, noting that “patients can have stages of
encephalopathy that come and go, which may explain why his abnormal EEG subsequently
improved, and now that he is having progressive upper extremity symptoms, the EEG would again
be abnormal.” Id. at 4.
Dr. Aalbers noted that AGS was incredibly rare. Ex. 55 at 4. He discussed that H.H.’s
thallium levels were elevated and this could “inhibit glutathione levels and cause similar symptoms
of encephalopathy” to AGS. Id. Dr. Aalbers recommended that H.H.’s parents discontinue all
homeopathic medications until thallium levels could be resolved. Id. In the context of AGS, Dr.
Aalbers noted that H.H. was likely in the early onset of the disease and repeat imaging could now
show evidence of early-onset leukodystrophy. Id. He also ordered testing for H.H.’s CSF interferon
alpha. Id.
Accordingly, H.H. underwent an EEG on the same date. Ex. 53 at 12. Dr. Fernando Acosta,
interpreting the results, stated that “this is an abnormal EEG due to mild generalized background
slowing. This may be consistent with an encephalopathic state. No electrographic nor
electroclinical seizures were recorded.” Id.
14
On December 20, 2013, while still in the hospital, H.H. was seen by Lori Thompson, CPNP
for a consultation regarding his elevated transaminases. Ex. 54 at 1. In the history of present illness
section, Ms. Thompson noted that H.H. had a “complex past medical history,” including
“abnormal newborn screening, concern[s] for a possible VLCAD”, and “metabolic genetics.” Id.
Ms. Thompson noted that the workup thus far had been “within normal limits.” Id. She noted an
unremarkable family history. Id. Upon a musculoskeletal examination, she noted “diminished deep
tendon reflexes over lower extremities, spastic tone. His tone is spastic, dynamic, dystonic, and
posture has hypotonia.” Id.
In the medical history, Ms. Thompson noted that H.H. “was a normally developing male
until approximately 15 months of age and he began losing milestones. He cannot walk, sit up, roll
over. He lost his verbal skills, but he is able to babble and is being followed by neurology for
progressive dystonia.” Ex. 54 at 1. She noted that AGS was a concern and that H.H. was being
“worked up by neurology” and by gastroenterology to follow his liver transaminases and evaluate
for the source of the elevation. Id.
On January 2, 2014, NMG labs reported the results of the repeat neurotransmitter studies
ordered by Dr. Aalbers on December 3, 2013. Ex. 52 at 71. H.H.’s neopterin was elevated, with a
value of 270 nmol/L (reference range 7-65 nmol/L), while his tetrahydrobiopterin was also
elevated, with a value of 69 nmol/L (reference range 18-58 nmol/L). Id. Dr. Hyland, interpreting
the results stated that “the concentrations of tetrahydrobiopterin and neopterin were above our
reference ranges. Elevations of neopterin and tetrahydrobiopterin have been described in []
Aicardi-Goutières syndrome.” Id. at 72.
On January 6, 2014, MNG labs reported no abnormalities in H.H.’s sialic acid metabolism.
Ex. 52 at 69.
On January 14, 2014, H.H.’s HIV testing was returned as “non-reactive.” Ex. 52 at 39. His
urine sample contained elevated 3-hydroxybutyrate, elevated 3-hydroxyisobutyric, elevated 2-et-
30hpropionic, elevated methylsuccinic, and low 3-OH-3-methylgutaric. Id. at 40-41.
On January 16, 2014, H.H. visited Dr. Samson Cantu at Cook’s Children’s Hospital for his
abnormal liver enzymes. Ex. 55 at 9. Dr. Cantu noted that H.H. had a history of tethered cord
repair, hypertonia, elevated liver enzymes all of unclear etiology. “Pt has had an extensive work-
up thus far with inconclusive findings. Since release from hospital he has had no jaundice, and
increased bruisability …. He has intermittent constipation responsive to miralax.” Id. Dr. Cantu
also noted that H.H.’s liver ultrasound was normal. Id. Upon examination, Dr. Cantu observed
H.H. as developmentally delayed. Id. at 11. All other systems were normal, including H.H.’s back
following surgery. Id. Dr. Cantu planned to repeat the liver panel, check H.H.’s CK level and
potentially perform a liver biopsy, depending on the results of the liver panel. Id.
On January 17, 2014, Quest Diagnostics returned the labs ordered by Dr. Cantu. Ex. 80 at
8. Under “hepatic function panel”, H.H.’s globulin was measured low at 1.7 g/dL (reference range
2.1-3.5 g/dL), leading to a high albumin/globulin ratio of 2.8 g/dL (reference range 1.0-2.5 g/dL).
Id. His indirect bilirubin was low at 0.1 mg/dL (reference range 0.2-0.8 mg/dL). Id. His AST was
15
high at 117 u/L (reference range 3-56 u/L), and his ALT was high at 129 u/L (reference range 5-
30 u/L). Id.
On February 4, 2014, H.H. was seen by Dr. Warren Marks to review the results of his
testing with genetics and neurology. Ex. 56 at 1. Dr. Marks indicated to H.H.’s father that H.H.’s
likely diagnosis was AGS and they were awaiting genetic confirmation. Id.
On the same day, H.H. visited Dr. Crawford at Cook Children’s Hospital, Department of
Clinical and Metabolic Genetics to discuss his disease and diagnosis. Ex. 50 at 23. Dr. Crawford
stated that “[H.H.] has had 2 lumbar punctures that showed an elevated neopterin. This is seen
only in Aicardi-Goutieres syndrome (AGS) and HIV infection. We ruled out HIV infection and
pursued testing for AGS…” Id. at 24. Dr. Crawford noted that blood testing and CSF both “showed
elevated levels of IFN-alpha which is diagnostic for AGS.” Id. In discussing H.H.’s possible
diagnosis with his family, Dr. Crawford stated that
[H.H.] appears to be hav[ing] a later-onset presentation for AGS as he presents after
a long period of normal development. He then presented with developmental
regression and developed progressive dystonia that is characteristic of the disease.
This disease can lead to a severe encephalopathy that can result in severe
intellect[u]al disability and physical disabilities. There is a spectrum for this
disease, so ther[e] are milder cases that have been reported in the literature
depending on which gene is involved. Typica[l]ly, these children have a regression
phase, followed by irritability, then a slow progressive encephalopathy phase.
These children[] typically develop peripheral spasticity, truncal hypotonia, dystonic
posturing upper limbs and poor head control, all of which [H.H.] is currently
displaying.
Id. Dr. Crawford noted that Dr. Crow’s lab in England was working on DNA testing to determine
which of H.H.’s genes were involved in his disease. Id. She noted that AGS is “now known to be
associated with mutation in 6 different genes.” Id. Dr. Crawford stated that “there are currently no
treatments known to affect or slow disease progression” and the H.H. would need “to continue
aggressive therapies due to his hypotonia and dystonia.” Id.
Regarding AGS in particular, Dr. Crawford noted that it is an “autosomal recessive
disorder, therefore recurrence risks for future pregnancies is 25%.... Therefore, if DNA testing
confirms [H.H.] is affected, parents are obligate carriers.” Id.
On March 6, 2014, Petitioner received the results of H.H.’s genetic testing. Ex. 50 at 40.
Only one significant mutation was found, a VLCAD deficiency in the gene ACADVL. Id. at 42.
On the same date, H.H. was seen by Dr. Marks for evaluation. Ex. 56 at 18. Dr. Marks
noted that H.H.’s eyes were “clear and anicteric and non cooperative with fundoscopic testing.”
Id. He observed H.H. to be “awake (but not very interactive)” and that he was nonverbal. Id. Upon
conducting a motor examination, Dr. Marks noted “motor spastic, rigidity, hypotonic axial,
hypertonia appendicular, and dystonia diffuse (and severe generalized dystonic posturing - trunk
and extremities with rigidity).” Id. He was non-ambulatory, and had decreased range of motion in
16
his spine. Id. Dr. Marks noted that the diagnosis for H.H. was still “possible AGS” but “with
negative genetic markers thus far.” Id. at 19. Dr. Marks also considered a retroviral infection as a
possible cause. Id. He noted that H.H. suffered from extreme irritability and ordered further testing.
Id.
On March 13, 2014, H.H. was seen by Dr. Kenneth Collins for an infectious diseases
consultation. Ex. 57 at 1. Dr. Collins noted that he was “consulted because [H.H.] is being referred
to the infectious diseases clinic over the next couple of weeks for possible retroviral infection
causing developmental delay.” Id. Under medical history, Dr. Collins noted that H.H.’s “mother
reports that she breastfed consistently until 10/09[/2013]. Within a day or 2 of stopping
breastfeeding he seemed to trip and fall when he was crawling.” Id. Dr. Collins noted that HH.’s
mother reported that H.H. was “completely normal” at his 15-month checkup. Id. Following the
checkup, she “stopped breastfeeding, and within a week he was falling. About 8 days later, after
stopping breastfeeding, he got his 15-month shots. After that time he developed increased inability
to crawl and this progressed over the next couple of months.” Id. Under a review of systems, Dr.
Collins noted that after H.H. “started falling in mid-October his parents noticed that he had a fever
for about a week, with a red throat that resolved.” Id.
Upon examination, Dr. Collins noted that H.H. was irritable, made good eye contact, and
appeared hypertonic. Ex. 57 at 2. His impression was “progressive dystonia with regression of
developmental milestones from 10/2013 through the end of 12/2013, with no improvement in
milestones since then. He is now not eating very well and requires a G button” Id. at 3. He also
had “continuous elevation in liver enzymes with negative hepatitis, cytomegalovirus, and Epstein-
Barr virus serologies.” Id. Dr. Collins wanted to recheck H.H. for HIV, but he thought it was
unlikely that this was the explanation for H.H.’s condition.
On the same date, H.H. was evaluated for placement of a G button. Ex. 58 at 1. It was noted
that “over the last 2 weeks, he is refusing to eat or drink very much. He maybe drinks 6-10 ounces
of PediaSure per day and not really eating unless mom forces him to.” Id. H.H. was also
dehydrated, urinating 2 times per day “in the last 5 days.” Id. He had also lost three pounds since
his 15-month checkup. Id.
On March 15, 2014, H.H. underwent surgery for insertion of a gastrostomy tube. Ex. 59 at
1. H.H. was noted as tolerating the procedure well and the operation was successful. Id. at 2.
On March 25, 2014, H.H. was seen for a lumbar puncture for diagnostic studies. Ex. 56 at
38. Dr. Marks noted that H.H.’s working diagnosis “has been Aicardi-Goutieres syndrome versus
retroviral infection based on his markedly elevated CSF neopterin levels.” Id. Various samples
were taken for neurotransmitter and other testing. Id.
On March 27, 2014, Dr. Marks received the results of H.H.’s updated neurotransmitter
testing. Ex. 56 at 358. H.H.’s neopterin was extremely elevated at 239 nmol/L (reference range 7-
65 nmol/L) and his tetrahydrobiopterin was also elevated at 75 nmol/L (reference range 18-58
nmol/L). Id. Dr. Hyland, the Ph.D. who interpreted the testing, noted that these findings were
consistent with a diagnosis of AGS. Id. at 363.
17
On March 31, 2014, H.H. was seen by Dr. Jason Kennedy at Cook Children’s Hospital,
Department of Orthopedics Services for neuromuscular decline. Ex. 60 at 1. Dr. Kennedy noted
that H.H. suffered from a “yet undiagnosed neuromuscular decline.” Id. Interpreting an AP pelvis
radiograph, Dr. Kennedy noted that H.H. had “encased tone throughout his upper and lower
extremities” and could “achieve a plantigrade position of the feet.” Id. He noted that H.H. had
“increased tone at his hip abductors and [had] increased neck-shaft angles on the x-ray” and his
“Shenton’s lines appear[ed] intact.” Id. Dr. Kennedy ordered a repeat AP pelvis radiograph in six
months. Id.
On April 17, 2014, H.H. visited Dr. Cantu. Ex. 61 at 12. Dr. Cantu noted that H.H. had a
“history of hypotonia of unclear etiology” and that he had an “extensive work-up by neurology
with unclear diagnosis, although it has been suggested he may have a variant of Aicardi.” Id. at
13. H.H.’s parents reported that “over the past few weeks, he has begun to [spit]-up/reflux much
more often” and that they were concerned with his level of reflux. Id.
On April 22, 2014, H.H. visited Dr. Marks for follow up regarding neurological regression.
Ex. 56 at 329. Dr. Marks noted that H.H. did “not have words at 19 months” and his “affect has
become more flat.” Id. at 330. He was diagnosed with “progressive encephalopathy and dystonia
with loss of milestones and worsening dystonia. Interferonopathy with elevated [sic] neopterin
clinically suggestive of Aicardi-Goutiere[s] Syndrome.” Id. at 333.
On May 21, 2014, H.H. was seen by Dr. Kyriacos Panayides because the neurology
department wanted a port added to his G button for IVIG treatments. Ex. 59 at 4. The medical
records note that H.H. was throwing up about thirty minutes after feeding. Id. He had pain during
feedings and was irritable at night. Id. A pH probe study was scheduled to attempt to locate the
source of the issue; H.H. had no fever or associated symptoms. Id. Dr. Panayides diagnosed H.H.
with “gastroesophageal reflux that is not responding to medical treatment.” Id. He ordered a UGI
study, noting that “if there is horrid reflux, a fundoplication will be performed at the same time as
the port. If the UGI is equivocal then a formal pH probe study will be done when the port is placed.”
Id.
On May 23, 2014, H.H. was seen by Dr. Jane Keng for consultation regarding feeding
intolerance, vomiting and pain behaviors. Ex. 62 at 1. Nurse notes from that date indicate that the
reflux was not acidic in nature. Ex. 63 at 1. Dr. Keng noted that H.H.’s CBC was normal, sodium
was 147, and his bicarbonate was 21. Id. at 2. She noted that his AST was elevated at 119 and his
ALT was elevated at 125. Id. Dr. Keng’s impression was that the intolerance, pain, and vomiting
may be due to gastroesophageal reflux disease and she suggested that H.H. be placed on external
pain medication rather than IV morphine. Id.
On June 23, 2014, H.H. was admitted to the hospital for a follow up with Dr. Marks after
placement of his gastronomy feeding tube. Ex. 56 at 325. A review of his mental status noted that
he was “awake (but not very interactive).” Id. at 328. He was nonverbal. Id. A motor system exam
revealed “motor spastic, rigidity, hypotonic axial, hypertonia appendicular (and severe generalized
dystonic posturing – trunk and extremities with rigidity).” Id. His reflexes were “1+ equal
throughout and brisk throughout.” His plantar reflex was “upgoing bilaterally (spontaneous
extensor responses).” Id. H.H. was “unable to perform heel-to-shin bilaterally.” Id. He was noted
18
to have “prominent scissoring.” Id. He was non-ambulatory and had decreased range of motion in
his spine. Id. His abdominal surgical wound was partially healed. Id. He was assessed with
“progressive encephalopathy and dystonia with loss of milestones and worsening dystonia.
Interferonopathy with elevated neopterin clinically suggestive of Aicardi-Goutiere[s] Syndrome
but with negative genetic testing by two different labs.” Id. Dr. Marks stated that because of the
negative genetic testing, he was “inclined to try several months of IVIG treatment.” Id. He noted
however, that after a literature review, it did “not appear that IVIG, steroids, [or] azathioprine
[would be] particularly effective” if H.H. did in fact have AGS. Id. at 329. Nevertheless, H.H.
began IVIG treatments in June 2014 which lasted for six months. Id.
On October 6, 2014, H.H visited Dr. Kennedy for a follow up. Ex. 60 at 25. Dr. Kennedy
discussed with H.H.’s parents that H.H. had “neuromuscular hip dysplasia and increasing
migration.” Id. Dr. Kennedy suggested Botox in the gastrocsoleus complex as treatment. Id.
On November 3, 2014, H.H. was seen for a lumbar puncture and Botox injections. Ex. 56
at 84. In a patient history obtained from H.H.’s mother, it was noted that H.H. developed “sudden
regression after vaccines at 15 mo[nths] old.” Id. at 104. Nurse notes from that date also indicate
that H.H. suffered from an “autoimmune response to vaccines.” Id. at 106. The notes from the
procedure indicate that H.H. “has laboratory findings consistent with Aicardi-Goutières
syndrome.” Id. Dr. Marks noted that H.H. had “been on 6 months of IVIG therapy and is here for
follow [] up studies.” Id. Labs conducted that same day revealed that H.H.’s IGG serum was
elevated at 2280 mg/dL (reference range 407-1009 mg/dL) and his CSF IGG/albumin ratio was
elevated at 0.26 (reference range 0.09-0.25). Id. at 92. His neopterin was extremely elevated at 300
nmol/L (reference range 7-65 nmol/L) and his tetrahydrobiopterin was elevated at 87 nmol/L
(reference range 18-50 nmol/L). Id. at 93.
On February 4, 2015, H.H. was seen by Dr. Michel Fayad at Boston Children’s Hospital.
Ex. 97 at 3. It was noted that H.H. had a history of regression at the age of 15 months and “the
regression happened around the time of his immunizations.” Id. at 2. Dr. Fayad noted that neither
metabolic work-ups or genetic work-ups showed any results and the possibility of an autoimmune
process was still something to look into. Id. at 3. Upon examination, he noted that H.H. was unable
to sit, crawl, or roll over, but socially he was “very interactive.” Id. at 2.
On March 6, 2015, Dr. Marks provided a letter stating that he was the “pediatric neurologist
caring for [H.H.].” Ex. 56 at 294. He stated that H.H. had been seen in the neurology clinic for
“autoimmune encephalitis” and that “he has received IVIG infusions.” Id. Dr. Marks also noted
that H.H. “has a gastrostomy tube for feeding.” Id. at 33.
On March 20, 2015, H.H. was seen by Dr. Lesley Hall, Dr. Miriam Bloom, Dr. Sally Evans,
Dr. Adeline Vanderver, and Amy Fizzino, MGC at the Myelin Disorders Clinic. Ex. 81 at 1. In
summarizing the visit, Dr. Vanderver noted that H.H. was seen “in the context of developmental
delay, dystonia, abnormal MRI and elevated CSF interferon/neopterin/tetrahydrobiopterin with a
clinical diagnosis of Aicardi Goutieres Syndrome, but negative genetic testing and no visible
intracranial calcifications on an early CT scan.” Id. In summarizing H.H.’s clinical picture, Dr.
Vanderver noted that:
19
[H.H.] [h]ad been fine until about 15 months of life, hitting all milestones on time.
In late October he had his 15-month vaccination (dTaP, flu, pneumonia).
Approximately a week later his crawling was deteriorating. He also had a fever of
about 102. Two weeks later he had rapid decline of motor function over 4 days,
with loss of ability to crawl, sit, talk, or use his arms purposefully. He was
extremely irritable. Per parents recollection he was not encephalopathic.
Id. Dr. Vanderver further noted that IVIG treatments beginning in June 2014 and lasting six months
“did not seem to improve things significantly.” Id. Dr. Vanderver noted that since that time, H.H.
had been “fairly stable” and possibly even showed improvement in August 2014, “where he started
to try to support himself in sitting and reaching for objects” as well as trying to use language. Id.
at 2. Dr. Vanderver noted that H.H. does, however, continue to have significant crying and
apparent discomfort. Id. Family history, birth history, and social history were reviewed and found
to be unremarkable in relation to H.H.’s symptoms. Id. at 3-4.
Upon examination, Dr. Vanderver noted that H.H.’s sleep was “poor” with multiple
awakenings during the night with crying. Ex. 80 at 2. H.H. also presented with sweating and a
faster respiratory rate while crying. Id. His parents estimated that he cried about thirty percent of
the day. Id. H.H. had dystonic posturing and crying, occasionally with…myoclonic jerks. Id. His
neurologic examination showed that H.H. was able to “briefly regard” the examiner, but he had
“no vocalizations with communicative intent and did not demonstrate receptive skills” during the
examination. Id. at 4. Dr. Vanderver’s impression was “developmental delay, dystonia, and
encephalopathy.” Id. at 6. Dr. Vanderver planned to follow up with Dr. Crow (AGS expert) to
facilitate genetic resolution of H.H.’s suspected heritable interferonopathy. Id.
On April 1, 2015, H.H. was seen by Dr. Eric Hubli for an enlarged soft palate. Ex. 76 at
23. Dr. Hubli did not see signs of an enlarge palate, but saw signs of a possible upper airway issues
for which he recommended a pulmonary evaluation. Id. at 26.
On April 2, 2015, H.H. visited Dr. Michelle Marcincuk for a sleep consultation due to his
persistent snoring. Ex. 72 at 13-14. In the HPI, Dr. Marcincuk noted the following was “reported
by parent”: “Pt got vaccines about 1.5 years ago. Within 3 [] months had dev regression.” Id. at
14. She noted that per H.H.’s mother, genetic testing was negative. She noted that Dr. Hubli (seen
on April 1, 2015) believed he had low muscle tone and currently suffered from dysphagia due to
low muscle tone. Id. Upon examination, she noted that his affect was “consistent with
encephalopathy” and that he suffered from hypotonia and spasticity. Id. Dr. Marcincuk diagnosed
H.H. with obstructive sleep apnea and hypertrophy of his tonsils and adenoids. Id. Dr. Marcincuk
explained to H.H.’s parents that corrective surgery would likely be required. Id.
On April 14, 2015, H.H. was seen by Dr. Sami Hadeed for complaints of stridor. Ex. 69 at
21. In the patient history, Dr. Hadeed completed notes, which summarized a history provided by
Mrs. Heller. These notes indicate that H.H. was “reportedly in perfect health until 15 months of
age when he developed neurological problems that his parents attributed to immunization. [H]e
was subsequently diagnosed with autoimmune encephalitis.” Id. at 22. H.H.’s parents stated that
H.H. had “noisy breathing” since birth, but this had gotten “markedly worse since he developed
neurological problems specially since December.” Id. H.H. had been seen by Dr. Marcincuk, who
20
diagnosed him with tonsillar and adenoidal hypertrophy, and recommended a tonsillectomy and
adenoidectomy, along with a flexible fiberoptic bronchoscopy. Id. Upon examination of H.H.’s
lungs, Dr. Hadeed noted “retractions, intercostal retractions, subcostal retractions, and strider
inspiratory and clear to auscultation and no distress.” Id. at 24. A review of H.H.’s musculoskeletal
systems indicated “contractures”, and an examination of his reflexes showed abnormalities of his
deep tendon reflexes. Id. Dr. Hadeed assessed H.H.’s stridor as secondary to pharyngomalacia and
his snoring as suggestive of a severe obstructive sleep apnea. Id. at 25.
On April 23, 2015, H.H. was seen by Dr. Cantu for a follow up of his feeding problem and
gastroesophageal reflux disease. Ex. 80 at 23. In the history of present illness, Dr. Cantu noted that
H.H. had a history of developmental delay, static encephalopathy, swallow dysfunction, and
gastrostomy-tube dependence. Id. Per H.H.’s mother, he was gaining weight well. Id. at 24. H.H.
was in a wheelchair. Id. at 25.
On April 27, 2015, H.H. was seen for a follow up with Dr. Kennedy. Ex. 60 at 14. In
interpreting an AP pelvis radiograph, Dr. Kennedy noted that H.H. “appeared to have more well-
seated hips today” and his tone was “much improved.” Id.
On April 28, 2015, H.H. was admitted to the hospital for several procedures. Ex. 72 at 1.
H.H. first underwent a bronchoscopy. Ex. 69 at 19. The procedure went well, and H.H. was
diagnosed with moderate to severe pharyngomalacia and moderate laryngomalacia. Id.
On the same date, H.H. underwent a successful tonsillectomy and adenoidectomy. Ex. 69
at 41, Ex. 72 at 4. He was admitted to the PICU following the procedure. Id. A physical exam the
next day revealed hypotonia and abnormal deep tendon reflexes. Id. It was also noted that he had
a swallow dysfunction. Id. at 45. An examination by Dr. Hadeed revealed that H.H. was in severe
pain but calmed down following administration of morphine. Ex. 70 at 13. In the HPI, Dr. Hadeed
noted that H.H. had suffered from autoimmune encephalitis since 15 months of age. Id.
On April 29, 2015, labs were taken, measuring H.H.’s hemoglobin to be high, with a value
of 13.2 g/dL (reference range 11.5-13.0 g/dL). Ex. 72 at 9. His sodium bicarbonate was also high,
measuring at 7220 mm3 (reference range 1500-5000 mm3). His Eosinophils and Eosinophil Count
Test (EOC) was low, measuring at 10 mm3 (reference range 30-800 mm3). Id. In the interpretation
section of the results, it was noted that these findings were consistent with methicillin resistant
staphylococcus aureus. Id. at 10.
On the same date, H.H. underwent an allergy panel. Ex. 77 at 1-2. H.H was noted to be
allergic to cow’s milk. Id. at 2.
On April 30, 2015, H.H. was discharged from the hospital. Ex. 72 at 1. He was scheduled
for a sleep study a month later to observe if further surgery was needed. Id. at 2.
On May 3, 2015, H.H. was admitted to the hospital emergency room with fever, lethargy,
poor perfusion, mild hypoxemia and concern for sepsis. Ex. 69 at 1. Under pertinent medical
history during triage, nurse notes indicated that H.H. suffered from dystonia and encephalopathy,
along with “auto immune response to vaccines”, among other conditions. Ex. 71 at 14. H.H. was
21
given IV broad-spectrum antibiotics and admitted to the intensive care unit for further evaluation
and treatment. Id. While in the hospital, H.H. was treated for parainfluenza bronchitis, sepsis
syndrome, hypoxemia secondary to bronchitis, acute respiratory distress secondary to bronchitis,
acute respiratory failure, fever secondary to bronchitis, and severe pharyngomalcia. Id. His
hospital discharge records indicate that he suffered from autoimmune encephalitis and
encephalopathy and developmental delay secondary to autoimmune encephalitis. Id.
On June 24, 2015, H.H. was seen by Dr. Marks for a follow up appointment. Ex. 56 at 389.
His condition was largely unchanged. Id. at 389-391. At this point he was standing, albeit with
“max support.” Id. at 389.
On November 2, 2015, H.H. was seen by Dr. Kennedy for follow up of his hip dysplasia.
Ex. 95 at 67-68. His parents reported that they were able to get him on a horse for therapy and that
he was scissoring less. Id. at 68. Dr. Kennedy noted that his tone was increased throughout and he
had had good response to Botox, which may be useful to try again. Id. at 71.
On February 29, 2016, H.H. was seen by Dr. Kennedy for hip tightness. Ex. 95 at 59-60.
H.H. was non ambulatory and was extremely inflexible. Id. at 61-62. Dr. Kennedy recommended
Botox injections. Id. at 62.
On March 4, 2016, H.H. was seen by Dr. Marc Mazade at the infectious diseases clinic as
a new patient. Ex. 95 at 54, 57. It was noted that H.H. “stopped vaccines after 15 months due to
neurologic condition that developed after vaccine administration.” Id. at 56. The following patient
history was obtained from Mrs. Heller and entered into the notes section of the record by Dr.
Mazade:
[H.H.] is a now 3-year-old boy who was seen by Dr. Whitworth in pediatric
infectious diseases consultation as an inpatient on March 14, 2014 in regard to
dystonia and progressive developmental delay. He has subsequently been
diagnosed with encephalitis of an autoimmune nature presumably due to
vaccinations two weeks previously. He is referred back to Infectious diseases now
for possible recurrent C difficile infection. … His immunizations are on hold due
to the concern for immunologically mediated neurologic injury.
Id. at 57.
On May 18, 2016, H.H. was seen by Dr. Marks at the spasticity clinic Ex. 95 at 49. H.H.
was noted to be wheelchair bound, keeping his hands loosely fisted throughout the exam. Id. at 53.
His mother reported that normally he was able to open them easily. Id. Dr. Marks noted “dystonic-
type UE movements present. LEs scissor when he is lifted. Id.
On July 7, 2016, H.H. received Botox injections in his hips. Ex. 95 at 223. The procedure
was uneventful and H.H. was discharged home. Id.
On August 29, 2016, H.H. was seen by Dr. Kennedy for a follow up exam following a
Botox injection. Ex. 95 at 41-42. Dr. Kennedy noted that H.H. had “further migration of
22
progression of his neuromuscular hip dysplasia” and corrective surgery would soon likely be
required. Id. at 45.
On November 1, 2016, H.H. was seen by Dr. Abigail Collins at the Neurology Clinic at
Children’s Hospital Colorado for treatment with medical marijuana. Ex. 98 at 1. H.H. was still
wheelchair-bound at this time. Id. at 3. It was noted that H.H. had not been treated with
immunomodulatory therapies to address his ongoing inflammation. Id. at 5. A physical exam was
largely unchanged from previous exams, although it was noted that H.H. was having difficulty
with lateral tongue movements. Id. Dr. Collins suggested continuing a trial of medical marijuana
for tone. Id. at 6. She also strongly recommended that H.H, undergo immune-mediated treatments
(such as steroids or Rituximab) after her review of the medical records. Id.
On December 5, 2016, H.H. was seen by Dr. Kennedy following treatment in “Colorado
for treatment with distilled cannabinoids for his overall spasticity and neurologic function.” Id. at
38. Dr. Kennedy noted that he continued to have decreased range of motion to his hips, most
notably to his right hip. Id. at 39. H.H. had no issues with his spine. Id. Dr. Kennedy discussed
surgery for bilateral adductor releases and bilateral proximal femoral varus derotational
osteotomies with H.H.’s parents. Id. at 40. H.H. was scheduled for surgery on December 8, 2016.
Id.
On December 8, 2016, H.H. underwent surgery for bilateral adductor releases and bilateral
varus derotational osteotomies of the femora. Ex. 95 at 199. The procedure was uneventful and
H.H. was discharged home on December 12, 2016.
On December 21, 2016, H.H. visited Dr. Kennedy for a follow up after his hip surgery. Ex.
95 at 31. This was his first visit post-surgery. Id. at 34. Dr. Kennedy observed no complications
from his surgery and explained that H.H. could begin gentle therapy. Id. at 34-35.
On January 16 , 2017, H.H. again visited Dr. Kennedy for a follow up after his hip surgery.
Ex. 95 at 27. At this point, he had no weight bearing restrictions, but was still reluctant to fully
extend his hips. Id. at 30-31. H.H. was noted to be healing well and improving gradually with his
flexibility. Id.
On February 27, 2017, H.H. had another follow-up with Dr. Kennedy after his hip surgery.
Ex. 95 at 22. H.H.’s examination was fairly unremarkable and his mother reported continued
improvement in stretching of his lower extremities. Id. Dr. Kennedy noted that H.H. had tightness
in his “gastrocs”, but as he continued to improve, this should resolve. Id. at 26.
On May 1, 2017, H.H. visited Dr. Marks. Ex. 95 at 17. The medical record noted that he
stopped receiving vaccines “after 15 months due to [a] neurologic condition that developed after
vaccine administration.” Id. at 18. H.H.’s mother clarified that he was up to date on all vaccines
except those normally received at four years old. Id.
On May 22, 2017, H.H. visited Dr. Marks for a follow-up 5.5 months post hip surgery. Ex.
95 at 15. He was noted to be “doing better” and making progress on his hip flexion contractures.
Id. at 16. Dr. Marks scheduled a follow up appointment for four months later. Id.
23
On June 26, 2017, labs ordered by Dr. Marks found H.H.’s glucose elevated at 121 mg/dL
(reference range 60-115 mg/dL). Ex. 95 at 77. A neurotransmitter study ordered the same date (but
reported on August 7, 2017) found H.H.’s neopterin levels to be normal, at 47 nmol/L (reference
range 7-65 nmol/L) and his tetrahydrobiopterin to be normal as well at 26 nmol/L (reference range
18-50 nmol/L). Id. at 78. All other results were also within normal ranges. Id. at 77-92.
That same day, H.H. underwent an MRI of his brain. Ex. 95 at 147. The MRI indicated that
H.H. had lost white matter volume over the past three years. Id. The corpus callosum was complete
but “quite thin”. Id. There was also “increased abnormal T2/FLAIR hyperintensity in the
periventricular white matter, extending into the centrum semiovale in the frontal regions and in the
periventricular white matter.” Id. Dr. Hayden Head, interpreting these results, noted that these
findings were concerning for a cerebral neurodegenerative process. Id. at 148. Finally, it was noted
that H.H.’s “maxillary sinuses are nearly completely opacified. There is also opacification of most
of the bilateral mastoid air cells.” Id. Dr. Head requested clinical correlation for sinusitis and ear
infection. Id. at 148.
On July 9, 2017, H.H. was seen by Dr. Jian Tong at Cook Children’s Emergency
Department with complaints of seizure. Ex. 95 at 105. The seizure started with “eyes twitching
then full body twitching upon ambulance arrival.” Id. Upon arrival of EMS, H.H. had “lip
smacking and eye rolling…and he also began to develop [] right upper extremity and then left
upper extremity tonic-clonic twitching.” Id. at 114. He had no history of seizures. Id. at 105. Under
medical history, it was noted that H.H suffered from “vaccine dystonia.” Id. The seizure lasted
approximately one hour and H.H. was reportedly playful and active prior to symptoms. Id. He had
no fever prior to the seizure. Id. Upon arrival at the emergency department, H.H. had a fever of
103o F, a white blood cell count of 21, and hypoxia, with O2 saturation 86% on room air. H.H. was
intubated. Id. Upon admission, H.H. was chemically sedated and paralyzed. Id. at 110. His O2
saturation was 97% on mechanical ventilation. Id. He had “coarse breathing sounds bilaterally.”
Id. He was also tachycardic. Id.
While still in the hospital, H.H. was seen by Dr. Ryan Meyer, who noted that H.H. had a
past medical history “significant for autoimmune encephalopathy thought to be vaccination related
with severe dystonia” at normal baseline prior to the onset of seizure. Ex. 95 at 114. Dr. Meyer
noted that a blood gas was obtained which revealed a pH of 6.97 and a CO2 of 111. Id. H.H. was
transferred to the PICU and continued to receive ventilation. Id.
Later that day, an electroencephalogram was conducted by Dr. Adrian Lacy. Ex. 95 at 126-
27. Dr. Lacy noted that H.H. was “a 4-year-old patient with a prior history of developmental delay
and dystonia, who is admitted with febrile seizure, manifesting with right face and arm clonus and
right eye deviation, as well as impaired mental status.” Id. at 126. Upon examination, Dr. Lacy
observed that “The hypersomnolence and generalized slowing seen in states of maximal
stimulation during the recording are reflective of diffuse nonspecific neuronal dysfunction as may
be seen in multiple encephalopathic or sedated states.” Id. at 127.
On July 10, 2017, Dr. Meyer observed significant improvement in H.H.’s condition. Ex.
95 at 133. An EEG taken overnight showed no seizure activity and no epileptiform activity. Id.
24
Dr. Lacy, also examining H.H. that day, stated that H.H. appeared to return to his prior baseline.
Id. at 134. Under impression, Dr. Lacy wrote:
This is a very interesting almost 5-year-old patient with a prior history of acute
encephalopathy with dystonia occurring at approximately 16 months of age, which
has been previously associated with vaccinations by parents, although the
significance of this is unclear, who has had extensive testing and have some
chemical parameters consistent with Aicardi Goutieres syndrome, for which the
range of onset and symptomatology may be relatively wide. However, the patient
does not have any gene mutations associated with this syndrome, and variants of
uncertain significance in his whole exome sequencing have not been shown to be
associated. He is being treated symptomatically for his dystonia, and recent
neuroimaging shows progressive white matter volume loss consistent with an
ongoing neurodegenerative process of uncertain origin…. The origin of the seizure
at this time is of uncertain cause, but the patient was not known to have fever prior
to the onset of seizure, and has not had fever since, has no evidence for encephalitis
currently by examination or by spinal fluid study. EEG is strongly suggestive of
postictal slowing in the left posterior temporal region, which is strongly concordant
with the patient's seizure semiology.
Id. at 135.
On July 11, 2017, H.H. was discharged from the hospital. Ex. 95 at 130. In the discharge
summary, it was noted that:
[H.H.’s] condition and new changes were discussed extensively with his attending
neurologist, Dr. Warren Marks. The management of Aicardi-Goutieres syndrome
is unclear, but it is felt by world-wide authorities that rituximab and other B-cell
immunotherapy is not effective. The management of seizures is not different with
Aicardi-Goutieres syndrome than with epilepsy syndromes. The plan arrived at in
discussion with Dr. Marks and family was for the patient to be discharged home
with Diastat to be used as rescue if needed, continue seizure precautions and first
aid and ER warnings, repeat EEG following discharge at baseline to evaluate for
need for initiation of antiepileptic therapy, and Dr. Marks will seek authorization
for a new medication, which is designed to inhibit the JAK-1 pathway, and
experimental use for AGS.
Id. at 131.
On August 23, 2017, H.H. was seen by Dr. Kennedy for a follow up appointment. Ex. 95
at 6. Dr. Kennedy noted H.H. liked to attempt standing. Id. at 10. He had had stem cell treatment
done in Panama, though H.H.’s mother reported no effect as of yet. Id. At the time, Petitioner was
still awaiting news from Dr. Vanderver or Dr. Crow regarding H.H.’s molecular diagnosis. Id.
On October 2, 2017, H.H. was seen by Dr. Kennedy for a follow up after his hip surgery.
Ex. 95 at 1. He was noted to be comfortable and his hip flexion contractures were improving. Id.
25
at 5. Dr. Kennedy noted that H.H. was not progressing towards ambulation at this point, although
he had “wide, symmetric abduction of the hips and [was] continuing to improve.” Id.
On November 29, 2017, H.H. visited Dr. Marks. Ex. 96 at 98. H.H.’s mother stated that at
the time, the only medication he was on was Botox. Id. at 101. She denied any new concerns
regarding H.H.’s condition. Id. at 102. Upon examination, Dr. Marks noted that H.H.’s hypertonia
seemed improved since his last visit. Id. He had bilateral Achilles contractures and his hips were
“very tight.” Id. He was “attentive and cooperative” and engaged well with others. Id. Dr. Marks’
assessment was “progressive encephalopathy and primary dystonia with loss of milestones and
worsening dystonia” and “interferonopathy with elevated neopterin clinically consistent [with]
Aicardi-Goutiere[s] Syndrome or other autoimmune mediated event.” Id.
On October 1, 2018, H.H. was seen by Dr. Marks for planned Botox injections in his lower
extremities. Ex. 96 at 1-2. Dr. Marks described H.H.’s condition as “autoimmune [encephalitis] –
presumed Aicardi Goutiere[s] syndrome.” Id. at 2.
On December 10, 2018, H.H. was seen by Dr. Marks for a neurologic exam. Ex. 96 at 5.
Dr. Marks noted that per his parents, H.H. had been less active since he received Botox injections,
with intermittent dilated pupils and coolness of his extremities. Id. H.H. was observed to be
somnolent and nonverbal. Id. His pupils were pharmacologically dilated and he had generalized
truncal hypotonia. Id. He had increased reflexes and bilateral striatal toes. Id. at 6. Dr. Marks noted
that H.H.’s dystonia was worsening. Id. Regarding AGS, Dr. Marks noted that H.H. had “negative
genetic testing by two different labs for all seven known AGS genes – however that only covers
95% of AGS cases.” Id.
On January 10, 2018, H.H. was seen by Dr. Kennedy for a pre-op discussion regarding his
G button and removal of hardware. Ex. 96 at 69. H.H.’s mother reported that he was “tight” in his
adductors. Id. Upon examination, his neurological condition was largely unchanged. Id. Upon a
musculoskeletal examination, Dr. Kennedy noted that H.H.’s hip flexion contractures were
improving, and that his ankles could be “fatigued to a neutral positioning.” Id. at 73. H.H.’s
radiographs showed that he had “well-seated” hips. Id.
On January 23, 2019, H.H. was seen by Dr. Marks. Ex. 96 at 10. Dr. Marks noted that H.H.
was deteriorating with motor regression – “severe quadriparesis dystonia/spasticity with bulbar
involvement.” Id. Dr. Marks noted that H.H. was “more alert” and his extremities seemed cool
rather than warm. Id. His examination was largely unchanged from December 10, 2018. Id. at 11-
12. Dr. Marks noted that H.H. did not have independent sitting and no standing, and that he
appeared lethargic. Id. at 11-12.
Dr. Marks noted that H.H.’s dystonia was currently being treated symptomatically. Ex. 96
at 13. He stated that the “best plan would be a JAK 1/2 inhibitor”, noting that he had discussed the
idea with Dr. Janik Crow and Dr. Vanderver (CHOP). Id. He also stated that “JAK 1/2 inhibition
would appear [to be] the best treatment even if [H.H.’s injury was] triggered by [an] immune
response to external stimulus such as immunization.” Id.
26
On the same date, H.H. was seen for an MRI of the brain. Ex. 96 at 15. Dr. Hayden Head,
interpreting, found “cerebral white matter volume diffusely moderately diminished, with
associated continued thinning of the corpus callosum.” Id. at 16. He also noted a “persistent thin
band of abnormal T2/FLAIR hyperintensity in the periventricular white matter” and “abnormal
T2/FLAIR hyperintensity with suspected volume loss of bilateral insula.” Id. Further, “the third
ventricle [was] substantially larger, while still maintaining a non-obstructed appearance.” Id. “The
lateral ventricles and fourth ventricle [were] mildly larger. The subarachnoid spaces and cerebella
fissures [were] newly prominent.” Id. Trace fluid was noted in the mastoid air cells, “markedly
decreased” from H.H.’s previous MRI. Id. Dr. Head’s impression was “enlargement of ventricles
and subarachnoid spaces” and he was concerned for progressive neurodegeneration. Id. He also
noted that there was “no significant change of already existing abnormalities” and that “for
Aicardi-Goutieres syndrome, the severity of findings is quite mild.” Id.
H.H.’s neurotransmitters were also measured at this visit. Ex. 96 at 14. His neopterin was
elevated at 176 nmol/L and his tetrahydrobiopterin was also elevated at 42 nmol/L.
On July 22, 2019, H.H. visited Dr. Shirley Tetteh at Cook Children’s Hospital Emergency
Department. Ex. 96 at 17. H.H. presented with “seizure-like activity” at home, for which his home
health nurse administered two doses of Diastat. Id. at 18. His mother stated that his seizure lasted
for about four hours and H.H. was febrile approximately two hours into the seizure. Id. Per the ED
nurse’s note, H.H. was actively seizing upon arrival. Id. Dr. Tetteh also noted that three weeks
prior, H.H. had received his third regimen of stem cell treatment in Panama. Id. H.H. was admitted
to the hospital. Id. Upon examination, it was noted that H.H. “appeared thin” and had increased
tone in both his upper body and lower body. Id. at 39-40. He also had abnormal muscle tone. Id.
at 40. H.H. was admitted to the hospital on the same date. Id. at 17.
On September 4, 2019, H.H. was seen by Dr. Marks and his MA, Ms. Kim Sunday. Ex. 96
at 56. His examination was largely unchanged from his neurological baseline. Id. at 58-60.
No additional medical records pertinent to this decision have been filed.
III. Petitioners’ Affidavits and Testimony
A. Affidavits
1. Heathe Heller
Mr. Heller is H.H.’s father. He testified that H.H. was born with no complications and was
otherwise healthy prior to his October 17 and 23, 2013 vaccinations. Ex. 64 at 1-2. H.H. was
developmentally on track for a 15-month old child. Id. at 2. H.H was “able to walk with one hand
assistance, crawl on his own, and climb.” Id. H.H. was also able to say some words like “Mama”
and “Dada”, and interact with family members by waving, kissing, and playing with the family
dog. Id.
The first time Mr. Heller noticed a change in H.H.’s health and behavior was one week
after his 15-month checkup where he had received his vaccinations and flu shot. Ex. 64 at 2. H.H.
27
lost the ability to do many of the things he had been able to do prior, including crawling, feeding
himself, talking, waving, and standing. Id. H.H. also seemed to be more irritable, and in a lot of
pain. Id. In early November of 2013, Mr. Heller remembered that H.H. ran a fever of 102º F for
two days and was recommended by Dr. Hollis to see a neurologist. Id. In December 2013, H.H.
was referred to many specialists and had many tests and procedures performed. Id. H.H. still does
not have a diagnosis but has general diagnoses of dystonia and encephalopathy. Id. at 2-3.
2. Jenna Heller
Mrs. Heller gave birth to H.H. with no complications and he was a healthy child who
experienced normal minor illnesses. Ex. 65 at 1-2. H.H. was a happy, outgoing, and energetic
child; he liked to play with golf clubs, hit golf balls, and play with the family dog. Id. at 2. Mrs.
Heller took H.H. to his 15-month vaccinations in October 2013, where he received his influenza
and DTaP vaccinations. Id. About a week after his vaccinations, H.H. ran a fever and his overall
health declined. Mrs. Heller took H.H. to Dr. Leslie Hollis, who referred him to specialists at Cook
Children’s Hospital. Id. Doctors and specialists have not been able to determine H.H.’s diagnosis
but he is being treated for dystonia and encephalopathy. Id. Mrs. Heller stated that “The only
possible cause for H.H.’s drastic and significant decline in health is a complication resulting from
the vaccinations he received at fifteen months, based on the timing and the severity of his
problems.” Id. at 3. It is devastating to see H.H. unable to do the things he used to love so much.
Id. H.H. is now in a wheelchair and requires a feeding tube to eat. Id.
3. Angela Kleinhans
Ms. Kleinhans is H.H.’s aunt. Ex. 92 at 1. Ms. Kleinhans stated that her daughter, H.H.’s
cousin, suffered from a vaccine reaction at her four month vaccinations so she has been aware of
potential side effects ever since. Id. at 2. Ms. Kleinhans stated that H.H. regressed so severely she
immediately thought it was related to his vaccinations. Id. Ms. Kleinhans also recalled that H.H.
was a very normal baby and met his milestones on time. Id. Ms. Kleinhans noted that “The
weekend after H.H. received his 15 months vaccinations he came down with a really high fever….
A few days [after October 23, 2013] he got sick and he was never the same again.” Id. Ms.
Kleinhans remembered receiving a call from Mrs. Heller to come to her house the weekend of
November 1st because she was worried about H.H. and he was now “doing this limp thing with his
leg.” Id. Ms. Kleinhans stated she saw H.H. two times each week after this date and saw H.H.
rapidly declining, from walking to limping, to crawling, and then crawling with his right leg
dragging behind him. Id. at 3. Ms. Kleinhans recalled that the family believed he had simply
injured his leg, but around November 8, 2013, Ms. Kleinhans saw that H.H. could no longer crawl
or sit up. Id. Ms. Kleinhans next recalled that H.H.’s hands “started turning in” and he could no
longer hold his head up on his own. Id. Ms. Kleinhans stated the Hellers took H.H. to the doctor
around November 13, 2013 and in the ensuing weeks, H.H. lost all speech, he would gag on all
food he ate, and he lost all motor skills. Id.
4. Sheri Huling
Ms. Huling signed her affidavit on March 21, 2016. Ex. 91. Ms. Huling is H.H.’s great aunt
and had worked as a pediatric physical therapist for 35 years as the time she signed her affidavit.
28
Id. at 2. Ms. Huling noted that H.H. was crawling, standing, and was able to take steps between
furniture before his vaccine on October 23, 2013. Id. Ms. Huling stated that a few weeks prior to
his October 23, 2013 vaccination, she noticed some tightness in his right heel cord that she directed
Mrs. Heller to bring up at H.H.’s next appointment. Id. Ms. Huling recommended some stretches
for Mrs. Heller to do with H.H. Id. Because H.H. was bearing weight on both legs, Ms. Huling
was not concerned. Id.
Ms. Huling next saw H.H. on October 31, 2013 for Halloween and noticed him fall over
when in a sitting position, and fall on a separate occasion when he was standing. Id. Ms. Huling
described a distinct memory where H.H. was standing in the family driveway as other children
were boarding a hayride and noticed H.H. “just falling down while standing.” Id. at 2-3. Ms. Huling
described receiving a call from Mrs. Heller on November 14, 2013. Id. at 3. Mrs. Heller was very
concerned because H.H. was unable to sit up or crawl and wanted Ms. Huling to see him so she
knew what to do. Id. Within two minutes of seeing H.H., Ms. Huling averred that she knew there
was a “serious neurological insult.” Id. Ms. Huling noted that H.H.’s trunk “was so hypotonic he
would just bend over forward while sitting on the floor and then could not right himself with his
arms.” Id. H.H.’s arms also could not support his body to crawl. Id. Everyone left for Cook
Children’s Hospital immediately. Id. H.H. continued to deteriorate over the next few months and
is now wheelchair dependent. Id.
Ms. Huling testified at the January 22, 2020 entitlement hearing noting discrepancies
between this affidavit and a letter she wrote to Ms. Guerra which served as the basis for her
affidavit. See Tr. at 205-07. Ms. Huling’s letter to Ms. Guerra was filed as Exhibit 102. In this
letter, Ms. Huling stated that H.H. was crawling, standing, and taking steps between furniture prior
to his vaccine on October 17, 2013. Ex. 102 at 1. After his pneumonia and flu vaccine on October
17, 2013, H.H. and Mrs. Heller visited Ms. Huling. Ms. Huling noticed that “over the last few days
[H.H.] was having some trouble cruising around furniture and taking steps and [Mrs. Heller] asked
me to take a look at him from a therapist perspective.” Id. at 1 (emphasis added). Ms. Huling
noticed that H.H. had right heel cord tightness that was alarming and told Mrs. Heller to bring this
matter up at H.H.’s next visit on October 23, 2013. Id. Ms. Huling next saw H.H. on Halloween
and noted worsening tightness in his right heel cord and described two instances where he fell
while sitting and standing. Id. The other details provided are similar to what was stated in her
affidavit. See generally id.; see generally Ex. 91.
B. Testimony
1. Heathe Heller
Mr. Heller testified at the January 22, 2020 entitlement hearing. Mr. Heller is a gas and oil
consultant in Midland, Texas. Tr. at 95-96. Mr. Heller described H.H.’s first year of life as fun
because he was such a playful child. Id. at 96. Mr. Heller did not accompany Mrs. Heller to the
vaccination appointments but his first recollection of something being wrong was when H.H.
began dragging his leg. Id. at 98. Mr. Heller also testified that he noticed something “was different”
on Halloween but couldn’t pinpoint a specific date regarding when H.H.’s leg dragging began. Id.
at 99. After Halloween, Mr. Heller remembered that H.H. would be playing, get tired, and lay
down; at some point the other leg started to give out as well. Id. at 100. Mr. Heller was not present
29
when Mrs. Heller drove to “Aunt Sher[i]’s” but remembered being at Cook’s Hospital emergency
room and talking to Dr. Aalbers. Id.
Mr. Heller testified that none of the doctors H.H. has seen have been able to give him a
diagnosis. Tr. at 103. H.H. is currently dependent on someone at all times. Id. at 104. H.H. now
has a full-time nurse and is able to go to school. Id. After the Hellers had another child, Mrs. Heller
spent more time with their new baby to breast feed him, so Mr. Heller slept with H.H. from 2013-
2017, until they moved to Midland and got his own room. Id. at 105-06.
2. Jenna Heller
Mrs. Heller testified at the January 22, 2020 entitlement hearing. Mrs. Heller is a licensed
professional counselor (LPC), working in the court system as a parenting coordinator and
performing custody evaluations for custody cases. Tr. at 7. Petitioners and their family moved to
Midland, Texas in 2017 for Mr. Heller’s work. Id. at 8. Petitioners have three sons, including H.H.
Id. H.H. was born with no complications but had an abnormal newborn screening with elevated
liver enzymes, which was resolved. Id. at 9. H.H. had some testing performed for his elevated liver
enzymes but the results ended up being negative. Id. at 10-11.
Regarding H.H.’s first year of life, Mrs. Heller testified she was a paranoid mom but had
no issues with H.H. Tr. at 11. Mrs. Heller took H.H. to Dr. Leslie Hollis for his 15-month checkup
and had concerns about whether his language skills were on track and also with him being “pigeon-
toed.” Id. at 13. Mrs. Heller stated she could not remember if it was his right leg or both legs that
turned inward. Id.
I asked Mrs. Heller about a phone call she made before H.H.’s 15-month appointment about
her concern about his ability to walk. Tr. at 15. Mrs. Heller stated she thought H.H. should be able
to walk more independently by 15 months but he would take a few steps and resume crawling. Id.
at 15. Mrs. Heller confirmed that she was concerned about his right foot turning inward on this
phone call as well. Id. at 15-16. Dr. Hollis assured Mrs. Heller that H.H. was developmentally in
range during the 15-month checkup and was meeting the appropriate milestones. Id. at 16.
Mrs. Heller testified that H.H. received two vaccinations on October 17, 2013, the flu and
pneumonia shots, and that the office had run out of Tdap vaccines so they scheduled for Mrs.
Heller and H.H. to return the following week to get the Pentacel vaccination. Tr. at 17. Mrs. Heller
said she noticed that H.H. had a fever the weekend after the vaccinations and slept the whole time.
Id. at 18. The following week was the week of Halloween which is when Mrs. Heller noticed he
was dragging his right foot and leg. Id. at 18-19. Mrs. Heller also remember arguing with Mr.
Heller because he noticed it first and thought H.H. had fallen and injured himself. Id. On
Halloween, other people noticed something off with H.H. because he typically stood with his
friends who are around the same age as he is, but he would just fall over and sit. Id. at 19-20. Over
the weekend, Mrs. Heller testified that his other leg started to drag as well, prompting Mrs. Heller
to call and schedule an appointment with Dr. Hollis. Id. at 20. Dr. Hollis “had no clue… what was
going on” but said H.H. needed to see a geneticist right away and got an appointment with Dr.
Heather Crawford. Id. at 21.
30
H.H.’s first appointment with Dr. Crawford was on November 5, 2013.13 Tr. at 21. Dr.
Crawford knew something was wrong but did not feel like H.H. needed to be admitted; she
instructed Mrs. Heller to see Dr. Hollis if he worsened. Id. at 22. During this appointment, Mrs.
Heller stated that H.H. could no longer crawl. Id. He could crawl during the weekend but one leg
dragged behind, which is why Mrs. Heller thought it could have been an injury. Id. at 23.
Between the two appointments with Dr. Crawford, H.H. went from being unable to crawl,
to being unable to sit up. Tr. at 24. Mrs. Heller immediately contacted her aunt, Sheri Huling, and
drove H.H. out to Decatur, Texas, where Ms. Huling lived. Id. at 24-25. Mrs. Huling did “some of
her PT things to try to figure out” what was wrong, and told them to go to Cook’s ER. Id. at 25.
Ms. Huling and Mrs. Heller’s mother drove them to Cook’s [Hospital] emergency department. Id.
Ms. Huling said something about H.H. not bending his legs, they were straight and scissoring, and
had a tight right (or left) heel cord, like a ballerina. Id. Dr. Aalbers was the neurologist on call at
the hospital so he is the one who observed H.H. upon arrival. Id. Dr. Aalbers believed H.H. was
experiencing dopamine responsive dystonia (DRD), and prescribed H.H. dopamine. Id. at 26, 27.
Mrs. Heller stated that the dopamine made H.H. very sick and did not help him at all. Mrs. Heller
remembered reporting back to Dr. Aalbers that the dopamine was not working around two weeks
after their visit. Id. at 28. Mrs. Heller testified that at some point, Dr. Aalbers called to inform her
that H.H.’s “brain cells are dying at a really rapid rate, and we don’t know why.” Id. at 28. The
next steps for H.H. was to have his whole genetic exome sequenced, which Dr. Crawford said
would take two to four months. Id. at 28-29. H.H. continued to get worse; he could pick up food
at one point but would bite his fingers when they were in his mouth. Id. at 29. At some point, H.H.
couldn’t bring the food to his mouth anymore and it would fall out of his hands prior to it reaching
his mouth. Id. H.H. was also not sleeping much at the time and was crying all the time; only over
time did the Hellers discover it was because he was in pain. Id. at 30.
Around three years, ago, in 2017, there was a huge turn around and it was “kind of like he
came out of this fog.” Tr. at 30. Dr. Hollis informed them that H.H. probably had a massive
migraine all the time and was cramping. Id. at 30-31. Somewhere around December 2013 or
January 2014, doctors were able to tell the Hellers that H.H.’s neopterin and tetrahydrobiopterin
levels were too high, and medical research could only find levels that high in HIV or AGS patients.
Id. at 31. Drs. Aalbers and Crawford explained that AGS was a very rare genetic disorder, more
common in Amish communities. Id. at 32. Mrs. Heller testified that she emailed Dr. Crow to get
H.H. tested for AGS around Christmas; Dr. Marks had told the Hellers about Dr. Crow and he was
the most specialized researcher of AGS. Id. H.H.’s first round of testing was negative and there
were six or seven known mutations of AGS at the time. Id. at 33. Another gene was discovered
after the petition was filed but H.H. was still negative for the new gene. Id. at 33-34.
H.H. continued to worsen and was given a G tube for his dehydration and eating issues. Tr.
at 34. H.H. had a consultation with Dr. Suzanne Whitworth, who asked whether H.H. had any
changes in his diet, to which Mrs. Heller informed her that she had weaned H.H. completely off
breastfeeding on October 9, 2013. Id. at 34, 37. Mrs. Heller clarified that H.H. did not deteriorate
after being weaned off of breastmilk but after his vaccinations. Id. at 37. Mrs. Heller also disputed
13
Later in her testimony, Mrs. Heller recognized that she had shifted these events one week forward. Tr. at
86.
31
Dr. Whitworth’s notation that H.H. started falling in mid-October and a “red throat and fever” that
lasted about a week. Id. at 40-41; see also Ex. 57 at 1. Mrs. Heller clarified she does not recall a
red or sore throat. Id. at 41-42.
Under Dr. Marks’ care, H.H. was immediately tested for AGS genes and he was started on
Baclofen. Tr. at 43. H.H. also had Botox injections and prescribed Thianicol and Clonidine. Id. at
43-44. Mrs. Heller testified that all these various treatments did not help or alleviate H.H.’s
symptoms. Id. at 45.
Mrs. Heller said she found out about vaccine injuries from her sister-in-law, whose
daughter had a vaccine reaction. Tr. at 46. Mrs. Heller said it was always in the back of their minds
because there were so many different avenues for them to pursue. Id. She kept suggesting things
to Dr. Marks so she must have mentioned the vaccinations as some point but Mrs. Heller doesn’t
know specifically when. Id. at 46. Dr. Marks would always call H.H.’s condition AGS-like and be
very vague. Id. at 47-48. Mrs. Heller recalled travelling to Boston and seeing a neurologist there
who told her he had never seen a patient like H.H. before. Id. at 49. Mrs. Heller then recalled going
to DC to do additional genetic testing, but the testing was also negative. Id. at 50.
Mrs. Heller testified that before the petition was filed, Drs. Marks and Crow were still
doing some testing but Dr. Marks told the Hellers that he believed that the vaccines triggered and
induced H.H.’s condition. Tr. at 51-52. H.H. had been repeatedly tested for the genes associated
with AGS which came back negative. Id. at 53. In 2015 (she later stated that it was during 2016-
2017), Mrs. Heller recalled H.H. coming out of a fog; within six months, his eyes were brighter
and seemed happier and would snuggle with his family members and move his arms to reach for
people. Id. at 53-54. The Hellers returned to Dr. Marks during this time, who was surprised at
H.H.’s improvement. Id. at 54-55.
Mrs. Heller testified that the first two years of H.H.’s condition were horrible but the last
two years (2017-2019) have been amazing. Id. at 55. The Hellers slept with H.H. until they had a
second child and they slept in entirely separate rooms. Id. at 56. The Hellers’ second child grew
up travelling with H.H. and going to all of this medical appointments. Id. Their second child had
to grow up quickly as a result. Id.
Regarding the November 11, 2013 visit with Dr. Hollis, the medical record notes that H.H.
had been fussy for the past week and had been experiencing developmental regression over the
last month. Tr. at 60-61. Mrs. Heller denied this record indicated H.H.’s developmental regression
began around October 11, 2013. Id. at 61.
Because there was some confusion with the timeline, Mrs. Heller then recounted what
occurred from her September 13, 2013 phone call to the November 11, 2013 appointment with Dr.
Hollis. Tr. at 63-66. Of note, Mrs. Heller stated that at some point after his vaccinations, H.H. ran
a fever and on a Monday morning, they went to see Dr. Hollis; on a Tuesday, they had an
appointment with Dr. Crawford; on Thursday, they went to Ms. Huling’s house and went to the
hospital. Id. at 65-66. Mrs. Heller also recalled having an argument with Mr. Heller the week of
Halloween because other people had noticed H.H. having issues. Id. at 66. Mrs. Heller testified
that all she could remember was H.H. slept throughout the weekend and “[b]y Halloween, he was
32
not running a fever anymore, because I wouldn’t have let him around his little buddies, his friends.”
Id.at 68. Between Halloween and when he was seen by Dr. Hollis, H.H. must have only
experienced leg dragging, otherwise she would have sought medical attention sooner. Id. at 68-69.
Mrs. Heller’s concern grew only when he was unable to sit up “that Monday morning.” Id. at 69.
There was a dramatic change between Monday and Thursday; H.H.’s legs were stiff, and his torso
was hypotonic. Id. Mrs. Heller was unsure if his fever occurred the weekend after his October 17,
2013 vaccinations or after the October 23,2013 vaccination. Id. at 70-71. Mrs. Heller testified that
around Halloween, H.H. could stand and he tried to play with his friends but he would fall over
and it “presented more like maybe at that time a virus kind of thing.” Id. at 72. The leg symptoms
occurred in his right leg and transferred to his left, then torso, arms, grasping, and the mouth was
last. Id. at 72-73. This progression lasted until the end of 2013, leaving H.H. nonverbal and unable
to chew. Id. at 73.
Mrs. Heller testified that H.H. now sees seven therapists, once or twice per week, and
regularly sees Drs. Marks and Hollis. Tr. at 87. H.H. has also had the same teacher for the past 2.5
years. Id. H.H. is able to communicate through his eyes, he can watch television, and he is happy
most of time. Id. at 87-88. H.H. still cannot move independently but he can move his arms to grab
people’s faces. Id. at 89.
3. Sue Sewell
Ms. Sewell is Mrs. Heller’s mother, grandmother to H.H. Tr. at 108-09. Ms. Sewell is now
retired but was a registered nurse, and worked as the chief nursing officer at a hospital in Decatur.
Id. at 109. Decatur is not far, so Ms. Sewell made almost weekly visits to the Hellers. Id. at 109-
10. Ms. Sewell accompanied Mrs. Heller to the October 17, 2013 appointment with Dr. Hollis
where H.H. received two vaccinations. Id. at 111. Ms. Sewell stated she remembered H.H. could
walk about two to three steps unassisted. Id. at 112. She also stated she did not remember any
conversation at the appointment regarding the turning inwards of H.H.’s right leg. Id.
Ms. Sewell testified that the weekend before Halloween, around October 26th, H.H. was
sleeping for many hours and she thought it was strange. Tr. at 113. She brought it up to Mrs. Heller
but they weren’t sure if it was an issue they should be concerned about. Id. Ms. Sewell also noticed
that H.H.’s legs did not really support him, and he kept falling over. Id. Ms. Sewell stated her
daughter, Mrs. Heller, would call nearly every day expressing concern that H.H. was not standing
anymore. Id. at 115. H.H. would try to feed himself but would end up biting his finger,
demonstrating he couldn’t coordinate his movements. Id.
On November 7, 2013,14 Ms. Sewell recommended Mrs. Heller take H.H. to her sister,
Sheri Huling, or Aunt Sheri, because she had been a pediatric physical therapist for 30 years. Tr.
at 115-16. Aunt Sheri did some tests with H.H., including putting him on all fours and having him
crawl to Mrs. Heller, but he couldn’t do these things. H.H.’s arms would collapse and he couldn’t
move towards Mrs. Heller. Id. at 116. Aunt Sheri told them they needed to go Cook’s (Hospital)
immediately and Aunt Sheri drove them because they were in shock. Id. at 117. Ms. Sewell
14
Again, this testimony shifted the visit to Cook’s Hospital forward. It is documented in the medical
records that H.H. did not visit the hospital on November 7, 2013.
33
accompanied Mrs. Heller to H.H.’s medical appointments when Mr. Heller could not. Id. The
Hellers’ lives have changed dramatically because of all the doctors they tried to take H.H. to,
around the country. Id. at 118-19. H.H. has never been able to get a diagnosis from any doctor. Id.
at 119.
4. Sheri Huling
Ms. Huling is H.H.’s great aunt, Mrs. Heller’s aunt, and Ms. Sewell’s sister. Tr. at 124.
Ms. Huling was a physical therapist for 38 years. Id. at 125. She received her degree from the
University of Texas Health Science Center. Id. Ms. Huling saw H.H. approximately every month
during his first year of life. Id. at 126. Ms. Huling had no concerns with H.H.’s early development.
Id. at 126-27.
Ms. Huling remembered Halloween very distinctly. Tr. at 128. The family was preparing
to go on a hay ride, and H.H. was standing in the driveway and just fell over. Id. Ms. Huling
examined him after he fell over and noticed his right ankle was tight. Id. Ms. Huling told Mrs.
Heller to inform his pediatrician. Id.
Ms. Huling received a phone call from Mrs. Heller on November 7, 2013,15 asking if she
could bring H.H. over. Tr. at 129. Mrs. Heller stated on the phone that H.H. kept falling over and
could not sit upright. Id. H.H. could not crawl and Ms. Huling told them to immediately go to
Cook’s hospital. Id. at 129. Ms. Huling’s first impression was that H.H. was experiencing some
type of encephalopathy because his problems appeared to be neurological. Id. at 130.
Ms. Huling testified about her affidavit (Ex. 91). Tr. at 130-34. Ms. Huling’s affidavit
stated she saw H.H. on November 14, 2021, but Ms. Huling stated she saw H.H. the same day he
went to Cook’s Hospital, and that her affidavit had an error. Id. at 134.
From a therapist’s perspective, Ms. Huling stated H.H. would need constant care the rest
of his life. Id. at 135. H.H. has made some improvements, as he has been able to feed without a
tube and can play some games. Id. at 136. Ms. Huling testified that she did not remember if Mrs.
Heller called her in September 2013 regarding the turning in of H.H.’s right leg.
Ms. Huling clarified that she saw H.H. after his October 17, 2013 vaccinations and noticed
the right heel tightness then. Id. at 139. Ms. Huling stated it was specifically “the week before the
23rd… I think it was the week before the 23rd.” Id. Ms. Huling was brought back to the stand to
confirm that she observed H.H. have right heel cord tightness before the October 23, 2013
vaccination. Id. at 205. Ms. Huling wrote a letter to Petitioner’s counsel to prepare her affidavit.
Id. Ms. Huling noted that H.H. exhibited normal crawling, pulling and standing, cruising, and
performed other physical acts prior to his October 17, 2013 vaccination and she had video footage
of it. Id. at 206. After the pneumonia and flu vaccines, Mrs. Heller and Ms. Huling noticed some
changes, and Ms. Huling instructed Mrs. Heller to bring up the right heel cord tightness when she
15
Ms. Huling also shifted the date of this visit forward approximately one week from its occurrence.
34
returned on October 23, 2013. Id. at 207. Ms. Huling’s letter to Petitioner’s counsel was admitted
into the record as Exhibit 97.16
IV. Expert Opinions and Qualifications
A. Petitioners’ Expert: Dr. Leslie Hollis
1. Qualifications
Dr. Hollis submitted a printout of her website’s “about me” page as her CV, in conjunction
with her affidavit. Ex. 66 at 4. Dr. Hollis received her medical degree from the University of
Oklahoma and performed her pediatric residency at [Baylor] Scott & White [Medical Center]. Id.
2. Affidavits
Dr. Hollis, H.H.’s treating pediatrician, filed two affidavits in this case. Exs. 66 (hereinafter
“First Hollis Affidavit”) and 90 (hereinafter “Second Hollis Affidavit”). In her first affidavit, Dr.
Hollis stated she has been H.H.’s treating pediatrician since his birth on July 14, 2012. First Hollis
Affidavit at 2. Dr. Hollis noted that H.H. was a healthy patient with no major issues; he had an
abnormal newborn screen which was retested and came back normal. Id. Dr. Hollis examined H.H.
on November 11, 2013, after he had been experiencing a fever of 101.5º. Id. She noted that at this
appointment, H.H. had noticeably less energy and his development “had been regressing over the
last month.” Id. at 2. Dr. Hollis referred H.H. to Dr. Heather Crawford, a metabolic genetics
specialist, and to an appointment with Dr. Brian Aalbers, a pediatric neurologist, for his
developmental issues. Id. Dr. Hollis continued to treat H.H. along with his other doctors. Id. It is
Dr. Hollis’ opinion that H.H.’s “rapid decline can be attributed to receiving the vaccinations on
October 17, 2013 and October 23, 2013.” Id. at 3.
Dr. Hollis’ second affidavit added a few more details regarding her history of treating H.H.
See generally Second Hollis Affidavit. Dr. Hollis stated that “H.H. has dystonia and neurological
impairment that manifested itself at 16 months of age.” Id. at 2. Dr. Hollis noted that H.H. was
assessed at 12 months of age and was within the normal developmental range for his age group.
Id. At his 15-month wellness check, Dr. Hollis noted that
he was taking a few steps independently between objects. His mom had noted his
foot possibly turning in 1 week prior to his appointment. The child was observed to
bear weight on both feet, and no significant intoeing was noted when he was trying
to walk. In my medical opinion, H.H. was still well within the developmentally
acceptable range for his age.
Id. Dr. Hollis next saw H.H. on November 11, 2013, where H.H.’s mother reported that his
development had been regressing over the last month; he stopped crawling, playing with toys and
eating table food. Id. Dr. Hollis immediately referred H.H. to neurology for evaluation of his
16
Because Petitioners did not file this letter, I prompted them to do so after the hearing. See informal
communication remark dated 3/15/2022; ECF No. 120. The letter was received as Ex. 102.
35
developmental regression. Id. Dr. Hollis further added that H.H.’s decline was severe and rapid
after his 15 month vaccinations and it was her opinion that H.H. will have “neurological and
physical suffering for the rest of his life.” Id. at 3.
B. Petitioners’ Expert: Dr. Warren Marks
1. Qualifications
Dr. Marks submitted a printout of his Cook Children’s Hospital physician page as his CV.
Ex. 67 at 6-7. Dr. Marks received his medical degree from Texas Tech University School of
Medicine and completed his residency and fellowship at the University of Oklahoma College of
Medicine. Id. at 6. Dr. Marks is board certified in neurology with a special qualification in child
neurology. Id. Dr. Marks has published two papers and 10 abstracts. Id. at 6-7. I recognized Dr.
Marks as an expert in pediatric neurology. Tr. at 146.
2. Affidavit and Expert Report
Dr. Marks filed one affidavit and one expert report in this case. Exs. 67 (hereinafter “Marks
Affidavit”) and 94 (hereinafter “Marks Expert Report”). In his affidavit, Dr. Marks noted that his
care of H.H. began on February 4, 2014, and that he had been treating H.H. for rapidly progressing
dystonia with encephalopathy. Marks Affidavit at 2. H.H.’s other symptoms included: acute
constipation, abnormal liver enzymes, encephalopathy, cough, dystonia, speech delay, and delayed
milestones. Id. Dr. Marks has performed many work-ups over the years and has ruled out over 20
different possible causes of H.H.’s condition, to include AGS, GBS, lysosomal storage disease,
Creutzfeldt-Jakob disease, heavy metal poisonings, Epstein-Barr virus, enteroviruses, and
cytomegaloviruses. Id. Testing done on H.H. includes extensive lab work, exome sequencing and
lumbar punctures. Id. Most testing was performed at Cook Children’s Medical Center though
testing for AGS was performed in England and France. Id. Dr. Marks opined that the start of H.H.’s
symptoms began after the receipt of his fifteen month vaccinations.17 Id. Dr. Marks further opined
that there is no other explanation for why H.H. developed severe and rapidly progressing dystonia
with encephalopathy at 15 months, other than his exposure to his 15 month vaccinations. Id. at 3-
4. Dr. Marks provided a theory as to how H.H.’s exposure to his vaccines caused his condition:
Essentially, H.H. was exposed to an antigen in the influenza or DTaP vaccines that
triggered a neurological deterioration and an abnormal movement disorder,
specifically dystonic posturing in his lower extremities which has rapidly
progressed throughout his body. Unfortunately, this Influenza or DTaP antigen
must have been similar to a “self” antigen in H.H.’s neurological structure, so that
a neurological deterioration also occurred. H.H.’s lab results showed elevated
levels of neopterin a marker of immune system activation, and tetrahydrobiopterin,
an enzyme used to produce serotonin, dopamine and other neurotransmitters.
Elevated levels of these enzymes have caused the interferonopathy, an up-
17
It should be noted that Dr. Marks did not observe or treat H.H. until he was more than 18 months old.
36
regulation of type-1 interferons, consequently resulting in his current symptomatic
state. The increase in interferons creates a sense that the body is under attack from
an outside source, but in H.H.’s case, there is no such source so the cause is only
neurological in nature H.H.’s neurological status has since stabilized, but still has
persistent increases in his interferon levels. This stabilization of his neurological
status, which was hyperactive post-immunization is indicative of the cause being
derived from the vaccinations…. Based on the timing of his vaccine inoculation
and the development of his symptoms thereafter, this theory makes complete sense
as a probable cause for his symptoms since there is no other explanation for the
sudden development or rapidly progressive dystonia with encephalopathy due to
the increased interferon levels in an otherwise previously healthy individual with
no other environmental exposures.
Id. at 4-5. Dr. Marks also opined that H.H. will suffer from dystonia and encephalopathy for the
remainder of his life and will require extensive continued medical treatment. Id. at 5.
Dr. Marks’ expert report was filed in response to Dr. Barañano’s first expert report. Ex. 94
at 1. Dr. Marks clarified that H.H. had been tested for the IFIH1 gene and was negative. Id. He
also confirmed that H.H. was negative for all known AGS genes and other non-genetic
inflammatory disorders like Lyme disease. Id. Dr. Marks’ report indicated that H.H.’s CSF
neopterin levels were normal, indicating the immune activation process may be normalizing but
extensive CNS damage has been done. Id. H.H.’s MRI in July 2017 also revealed no intracranial
calcifications or injury to the basal ganglia consistent with AGS. Id. Dr. Marks’ concluded that
there are two realistic options for H.H. at this point: he is one of the very rare cases of AGS without
a known genetic marker or he has an AGS-like interferonopathy triggered by “external immune
stimulating condition such as immunization.” Id. Given his normalizing neopterin levels, “I would
favor the latter.” Id.
2. Testimony
Dr. Marks testified at the January 22, 2020 entitlement hearing. Dr. Marks has practiced in
the field of pediatric neurology for 40 years and specializes in movement disorders, rehabilitation,
and neuromuscular disorders. Tr. at 140. Dr. Marks is H.H.’s treating pediatric neurologist. Id. at
141-42. Dr. Marks’ first visit with H.H. was in February 2014. Id. at 142. When Dr. Marks saw
H.H. on February 4, 2014, there was a presumptive diagnosis of Aicardi-Goutières syndrome based
on elevated neopterin levels in his spinal fluid. Id. at 146.
Dr. Marks testified that AGS is “a disorder of interferon activity… it’s an immune mediated
disorder that typically result[s] in neurologic regression with dystonia, intracranial
calcifications,… seizures… almost always have a skin rash of some kind.” Tr. at 147-48. H.H. did
not have a skin rash or calcifications on his neuroimaging. Id. at 148-49. AGS patients are also
more likely to have seizures. Id.at 149. With a working diagnosis of AGS, Dr. Marks sent H.H.’s
testing to be done by Medical Neurogenetics in Atlanta, which has a neurotransmitter gene panel
test for AGS. Id. at 149-50. H.H. was tested against then six known genes for AGS. Id. at 150. A
seventh gene was identified but H.H. tested negative for all seven genes. Id.
37
Dr. Marks had discussions with Dr. Yanick Crow, the world’s expert in AGS. Tr. at 150.
Samples were sent to France, where Dr. Crow’s research lab was located. Id. Dr. Crow confirmed
H.H.’s interferon levels were elevated. Id. H.H.’s entire genome was sequenced to find genes that
would explain his dystonia, AGS, and other symptoms, but this testing did not provide an
explanation for H.H.’s condition. Id. at 151. Dr. Marks gave H.H. a diagnosis of an “AGS-like”
disease because H.H. has many of the clinical manifestations of AGS but no genetic markers. Id.
Dr. Marks testified that he cannot prove H.H. does not have AGS, but noted that there is clinical
evidence to suggest it is not AGS as well. Id. The most recent terminology he has used to describe
H.H.’s condition is dystonia with interferonopathy. Id. at 153. An interferonopathy means H.H.
has an elevated level of interferon. Id.
Dr. Marks stated vaccinations are meant to cause an immune response and H.H.’s
symptoms began shortly after immunization. Tr. at 153-54. Dr. Marks additionally testified that
“it’s not unique for vaccine to cause immune responses that produce neurologic injury. Guillain-
Barre has been well known to be associated with vaccines off and on.” Id. at 154. Dr. Marks stated
that H.H. has had elevated interferon levels for six years, with some fluctuation, but it otherwise
indicates that there is a persistent immunologic response or a genetic defect. Id. at 155.
Dr. Marks also discussed H.H.’s case with Dr. Vanderver, the American expert on AGS,
and had the Hellers see her while she was working at Children’s National Hospital in Washington,
DC. Tr. at 156-57. Dr. Marks testified that Dr. Vanderver was not convinced H.H. had AGS and
H.H. could not participate in any trials because he did not have any genetic markers for the disease.
Id. Regarding H.H.’s current condition, Dr. Marks opined that H.H. has stopped regressing and
has been clinically stable for the last year because he has not lost any skills. Id. at 157.
Dr. Marks opined in favor of vaccine causation for several reasons. First, H.H. was a
normally developing child prior to his 15-month vaccinations. Tr. at 158. Second, there is a
temporal correlation between vaccination and H.H.’s deterioration. Id. at 159. Finally, H.H. has
no known no genetic marker that would explain his condition. Id.
For the 5% subset of AGS patients who do not a known genetic marker for AGS, they are
given the AGS diagnosis because they have other signs, like calcifications in the brain or skin rash.
Tr. at 160-61. H.H.’s onset at 15-months of age is significant in that later onset cases of AGS tend
to be milder. Id. at 161. Another difference in H.H.’s presentation is that he seems to have
stabilized; if this were a “triggered reaction,” it makes sense that it should wane over time. Id. Dr.
Marks opined that he did not expect an AGS patient to make improvements; it is a “relentlessly
progressive disorder.” Id. at 164.
Dr. Marks examined H.H. one day prior to the entitlement hearing and observed that he
was stable. Tr. at 166-67. Dr. Marks noted his condition had not changed; H.H. still has very severe
dystonia but he has a communication device that helps him interact and he is much less irritable.
Id. at 167. Dr. Marks confirmed his belief that either H.H. has a rare case of AGS without a known
genetic marker or he has an AGS-like interferonopathy “triggered by external immune stimulating
conditions such as immunization.” Id. at 170. Dr. Marks also testified that he does not know why
the vaccines were able to trigger such a sustained reaction, as he is not an immunologist. Id. at
170-71. Even in viral mediated diseases like Guillain Barré syndrome, the response is not sustained
38
over time. Id. Dr. Marks did not identify a specific vaccine he believed was more likely to be
causal. Id. at 173. Dr. Marks used Guillain Barré syndrome as a model when discussing the medical
appropriate time frame for when an immune mediate disease should develop, usually one to two
weeks after immune stimulus. Id. at 175-76.
Dr. Marks communicated with Drs. Crow and Vanderver mostly at conference meetings or
phone calls. Tr. at 177-78. Dr. Marks confirmed that Dr. Vanderver was unsure what condition
H.H. had but she noted that she believed H.H. likely has an inherited interferonopathy. Id. at 179.
Dr. Marks also confirmed that there was no literature submitted to support his proposed theory of
molecular mimicry in this type of case. Id. at 187. But Dr. Marks stated his theory was not specific
to molecular mimicry, just that an immune response was triggered as a result of the vaccinations
H.H. received. Id. at 188. We know that vaccines trigger an immune response, and on occasion,
“the immune system just goes wild.” Id. at 193. Dr. Marks testified that in his conversations with
Dr. Crow, Dr. Crow believed that AGS was the most logical diagnosis even though they could not
identify which gene caused H.H.’s condition. Id. at 203-04.
Dr. Marks testified that H.H.’s condition started when H.H. had a fever and was irritable.
Tr. at 195. I also asked Dr. Marks if I find onset of H.H.’s condition was prior to his 15-month
vaccinations, would his theory change. Id. Dr. Marks opined that the vaccinations could cause a
fever to develop which could be “enough to trigger an irreversible neurologic decline.” Id. at 196-
97.
C. Petitioners’ Expert: Dr. Lawrence Steinman
1. Qualifications
Petitioner filed Dr. Steinman’s CV on July 24, 2020. Ex. 101, Tab 1. Dr. Steinman received
his medical degree from Harvard University and was a NIH Fellow in Chemical Neurobiology at
Harvard Medical School. Id. at 1. Dr. Steinman completed his residency in pediatrics and pediatric
and adult neurology at Stanford University Hospital. Id. Dr. Steinman is the GA Zimmermann
Chair as Professor of Neurological Sciences, Neurology, and Pediatrics. Id. Dr. Steinman is board
certified in neurology and is involved in the American Academy of Neurology as a fellow, the
American Neurological Association, the American Association of Immunologists, and the Clinical
Immunology Society. Id. at 2. Dr. Steinman has over 40 patents (not limited to U.S. patents). Id.
at 2-3. Dr. Steinman has published nearly 600 articles. Id. at 5-48.
1. Post-Hearing Expert Reports
Petitioners filed two reports from Dr. Lawrence Steinman. Exs. 101 (hereinafter “First
Steinman Rep.”) and 99 (hereinafter “Second Steinman Rep.”). In his first report, Dr. Steinman
stated that his theory focuses on “how the components of the [Pentacel] vaccine can drive an
interferon response. It is not a theory based on molecular mimicry.” First Steinman Rep. at 9. There
are two types of interferons have different receptors but share common signaling pathways
including JAK and STAT molecules. Id. Type 1 interferons break down into other subtypes,
whereas Type 2 interferons are only broken down to gamma interferon. Id. The Pentacel vaccine
consists of many different components, including DTaP-IPV, ActHIB, and H. influenzae type b
39
bound to tetanus toxoid. Id. at 11. The pertussis toxin “induces immune responses to both gamma-
interferon and to type 1 interferon.” Id. at 12.
The Pentacel vaccine also contains alum, which activates the NALRP3 inflammasome,
“which plays a role in inducing interferonopathies.” First Steinman Rep. at 12. There are a number
of interferon responsive neuroinflammatory conditions such as multiple sclerosis (MS) and its
animal model, experimental autoimmune encephalomyelitis (EAE), and these conditions are tied
to strong activation of innate immunity induced by the NLRP3 inflammasome. Id. Dr. Steinman
also coauthored a paper about how Type 1 IFNs and type II IFN mediate both regulation and
inflammation in MS, neuromyelitis optica, and EAE; however “the underlying mechanism for
these Janus-like activities of type I and II IFNs in neuroinflammation remain unclear.” Id. at 14.
Dr. Steinman noted that “[a]lthough endogenous type I IFN signaling provides a protective
response to neuroinflammation, we find that when IFFN-g signaling is ablated, type I IFNs drive
inflammation, resulting in exacerbated EAE. Id.
Dr. Steinman stated that although H.H. does not have an ADAR-1 mutation, a vaccine
could still trigger his interferonopathy. First Steinman Rep. at 14. Dr. Steinman cited to Dr. Crow’s
paper (Ref. 18) which states that:
Indeed, considering a putative role of physical stressors, note should be made of
the cold dependency of the skin lesions seen in the type I interferonopathies and of
a striking temporal relationship between the onset of ADAR1-related bilateral
striatal necrosis and preceding infection. Whether vaccination represents a disease
trigger is an important, and currently unanswered, question. Meanwhile, the
possibility of a “cumulative” genetic burden contributing to cellular pathology is
notable in light of recently published data on the group of type I interferonopathies
caused by loss-of-function mutations in proteasome subunits.
Id.; see also Rodero & Crow, Type I interferon–mediated monogenic autoinflammation: The type
I interferonopathies, a conceptual overview, 213 J. EXP. MED. 12, 2527-38, 2351-52 (2016) (filed
as Ex. 101, Tab 18) (hereinafter “Rodero & Crow”). Dr. Steinman opined that the onset of H.H.’s
neuroinflammation within three weeks of the Pentacel vaccination is consistent with references 18
and 19. Id. at 15. Dr. Steinman further opined that the Pentacel vaccine significantly aggravated
H.H.’s prior condition which included the mild intorsion of his foot prior to the vaccination. Id. at
16.
Dr. Steinman filed a second expert report in response to Dr. McGeady’s report. Ex. 99. Dr.
Steinman stated that both experts agree that the genetic basis for H.H.’s interferonopathy remains
elusive, however the diagnosis of an interferonopathy is akin to AGS. Id. at 2. Where Drs.
McGeady and Steinman disagree is whether the Pentacel vaccine can trigger a “physiologic
amount of type I interferon.” Id. Dr. Steinman clarified that he believes that the vaccine is merely
a trigger for an interferon response. Id. The overproduction of interferon type 1 “can be explained
by the references which show that there is a resistance in some forms of neuroinflammation to the
normal beneficial response of interferon. So unchecked interferon production can drive
neuroinflammation.” Id.
40
Dr. Steinman added that if H.H. did have an underlying AGS condition, the Pentacel
vaccine would have worsened his neuroinflammation. Second Steinman Rep. at 3. Dr. Steinman
reiterated that it does not matter if H.H. had neurological symptoms prior to his 15-month
vaccinations, just that the Pentacel vaccine on October 23, 2013 caused neuroinflammation, which
could have significantly aggravated his condition, or caused his condition. Id. at 4.
D. Respondent’s Expert, Dr. Stephen McGeady:
1. Qualifications
Respondent filed an updated curriculum vitae for Dr. McGeady on April 4, 2020. Ex. I. Dr.
McGeady received his medical degree from Creighton University and completed his residency in
pediatrics at St. Christopher’s Hospital in Philadelphia, and his fellowship at Duke University in
psychiatry and allergy. Id. Dr. McGeady is currently a professor of pediatrics at Jefferson Medical
College and is the Emeritus Chief of the Allergy, Asthma & Immunology Division at duPont
Hospital for Children. Id. Dr. McGeady is board certified in pediatrics and allergy/immunology.
Id. Dr. McGeady has published at least 66 peer reviewed papers and 93 abstracts. Id. at 2-7, 7-13.
I recognized Dr. McGeady as an expert in pediatric immunology and pediatrics. Tr. at 213.
2. Expert Reports
Dr. McGeady filed two expert reports in this case. Exs. D (hereinafter “First McGeady
Rep.”) and J (hereinafter “Second McGeady Rep.”). In Dr. McGeady’s first report, he noted that
H.H. lacked some clinical features of AGS, such as calcification in the basal ganglia, chilblain-
like skin lesions, and pleocytosis in the CSF. First McGeady Rep. at 4. However, AGS literature
stated intracranial calcification should not be considered a prerequisite for an AGS diagnosis. Id.
Dr. McGeady also disagreed with Drs. Hollis and Marks’ assessment that H.H.’s normal
development until 15-16 months is incongruous with AGS. Id. at 4-5. H.H.’s fever is also
consistent with 405 of subjects in the Rice paper. Id. at 5. Markedly high neopterin and biopterin
levels are typically only seen in two disorders, AGS and congenital HIV. Id. Dr. McGeady also
noted that Dr. Vanderver believed H.H. has a “suspected heritable interferonopathy”, which is
consistent with AGS and inconsistent with an adverse vaccine reaction. Id. at 6; see also Ex. 81 at
10.
Dr. McGeady also opined regarding Dr. Marks’ proposed causal theory. First McGeady
Rep. at 7-10. Dr. McGeady stated that there are six possible metabolic lesions that have been
proposed to account for the excess production and/or accumulation of interferon alpha and none
of these mechanisms is “dependent upon immune activation alone.” Id. at 8. Dr. McGeady also
noted that H.H.’s medical history does not include any localized reaction to any of the vaccines he
received, which indicates no excessive reaction was produced. Id. at 9. Additionally, H.H. had
elevated transaminase levels, which are associated with AGS but have not been associated in cases
of patients who developed encephalopathies after vaccination. Id.
Dr. McGeady also pointed out Mrs. Heller’s 9/13/2013 phone call regarding H.H.’s
inturning of his right foot and inability to walk; he opined this may have been the first mention of
H.H. losing skills. Id. at 10. Dr. McGeady also addressed Dr. Hollis’ affidavit which broadly stated
41
she had never seen a similar loss of skills in a previously normal child, and based on the timing,
believed that H.H.’s condition was caused by his immunizations. Id. at 11. Dr. McGeady reiterated
that H.H.’s lack of genetic markers does not rule out AGS, considering his clinical and laboratory
findings. Id.
3. Testimony
Dr. McGeady provided testimony on molecular mimicry and testified that it is “intuitively
appealing” but in reality, almost never happens. Tr. at 214-15. There are many mimics widespread
in nature but there are not many autoimmune diseases linked to molecular mimicry in a frequency
one expects if molecular mimicry were real. Id. at 215-16. There are two accepted examples of
molecular mimicry, which include GBS and campylobacteria and more recently, narcolepsy with
the 2010 H1N1 flu. Id. at 216. There is no literature or case reports linking the flu and/or DTaP
vaccine to a Type 1 interferonopathy. Id. at 217. Nor are the viruses of these vaccines known to
cause a Type 1 interferonopathy. Id. at 218. Dr. McGeady testified that the only know causes of a
Type 1 interferonopathy are a genetic predisposition or intrauterine viral infections. Id. at 218-19.
In the case of an intrauterine viral infection, a Type 1 interferonopathy is caused when a
viral infection is “particularly persistent” like the HIV virus in a pregnant woman. Tr. at 220. The
fetus become infected as well and starts to produce large quantities of Type 1 interferon; the fetus
is extremely susceptible to the adverse effects of Type 1 interferonopathy and becomes badly
damaged as a result. Id. Both viral causation and genetically predisposed babies look similar even
when different etiologies exist. Id. Dr. McGeady testified that even if molecular mimicry were a
viable theory, he does not believe vaccinations could have triggered this kind of response. Id. at
223. Any triggered reaction could have an intense activation however “it gets damped down
quickly.” Id. Only in hereditary interferonopathies are there no breaks. Id. H.H.’s neopterin levels
have fluctuated over the years but there are no active organisms in the vaccines he’s received that
could cause this kind of neopterin production. Id. at 223-224. Molecular mimicry cannot explain
“something that perpetuates over six years.” Id. at 224. Molecular mimicry also pertains to the
adaptive immune system and there was no evidence of H.H. having an adaptive immune response,
or localized reaction, to the vaccinations. Id. at 224-25.
Dr. McGeady testified that he believed that H.H.’s lack of genetic markers does not mean
he does not have AGS; he noted that new genes and sub mutations are still being identified. Tr. at
228-29. Dr. McGeady opined that AGS is the condition most consistent with H.H.’s presentation.
Id. at 233. Dr. McGeady also testified that H.H.’s improvement is not inconsistent with AGS; some
patients have normal intellectual capacity and have courses that stabilize. Id. at 234.
4. Post-Hearing Report
Dr. McGeady’s second report was filed in response to Dr. Steinman’s first expert report
(Ex. 101). Dr. McGeady opined that Dr. Steinman’s proposed mechanism regarding how the
Pentacel vaccine caused H.H.’s condition is not consistent with what is known regarding type I
interferonopathies. Second McGeady Rep. at 1.
42
Dr. Steinman proposed that the Pentacel vaccine activated H.H.’s innate immune system
and the subsequent production of type I interferon and other inflammatory cytokines caused
damage to H.H.’s central nervous system. Second McGeady Rep. at 1. Dr. McGeady argued that
Dr. Steinman’s theory does not explain how this reaction caused elevation in interferon levels for
the past six years. Id. Vaccines are meant to trigger an immune reaction however, to trigger a
cytokine storm that is perpetuated over a number of years is unpersuasive. Id. at 2. Only in an
inherited interferonopathy are interferon levels elevated for the length of time seen in H.H. Id.
Dr. McGeady addressed Dr. Steinman’s second theory, that the Pentacel vaccine
significantly aggravated a pre-existing condition. Second McGeady Rep. at 1. Type I interferons
are produced by the innate immune system and are present in measurable quantities within 12
hours following a viral exposure. Id. Interferon production promptly decreases following a non-
progressive provocation, thus “it would be expected that an acute injury to the CNS due to
excessive type I interferon would appear sooner than several weeks following the immunization if
vaccines are to be suspected as the initiating event.” Id. H.H. suffered from many febrile illnesses
(on 12/10/2012, 5/20/2013, 7/29/2013, and 11/11/2013); these would have been suspected
initiating events as well. Id.
Dr. McGeady opined that the persistent elevations of interferon alpha and other markers of
type I interferonopathy cannot be the result of H.H.’s October 17 and 23, 2013 vaccinations.
Second McGeady Rep. at 3. Dr. McGeady reiterated that Dr. Steinman’s theory does not account
for the chronic overproduction of type I interferon. Id. Congenital type I interferonopathies do
produce enduring excess amounts of cytokines, as seen in H.H. Id.
E. Respondent’s Expert, Dr. Kristin Barañano
1. Qualifications
Respondent filed an updated curriculum vitae for Dr. Barañano on April 14, 2020. Ex. H.
Dr. Barañano received her medical degree and a Ph.D. in neuroscience from Johns Hopkins
University School of Medicine. Id. at 1. Dr. Barañano completed residencies in pediatrics and
pediatric neurology at Johns Hopkins University School of Medicine and was a research and
clinical fellow in neurogenetics at the Kennedy Krieger Institute. Id. Dr. Barañano is currently an
Assistant Professor of Neurology at Johns Hopkins School of Medicine and is Medical Staff at the
Kennedy Krieger Institute. Id. Dr. Barañano has published papers, case reports, book chapters and
editorials. Id. at 2-3. Dr. Barañano is board certified in neurology, with special qualification in
child neurology. Id. at 4. I recognized Dr. Barañano as an expert in pediatric neurology and
neurogenetics. Tr. at 252.
2. Expert Reports
Dr. Barañano filed two reports in this case. Exs. A (hereinafter “First Barañano Rep.”) and
C (hereinafter “Second Barañano Rep.”). In Dr. Barañano’s first report, she provided a typical
presentation of AGS but cited to AGS case studies that demonstrated a wide spectrum on onset
and presentations. First Barañano Rep. at 3. In Dr. Crow’s 2015 paper, 8.6% of patients presented
after one year of age, and this occurrence was more common with certain AGS-associated genes.
43
Id. at 3-4. Dr. Barañano also identified Mrs. Heller’s 9/13/2013 phone call as onset of neurological
symptoms with the in-turning of H.H.’s right foot and right heel cord tightness. Id. at 5. Dr.
Barañano testified that H.H. had a fever in between his vaccinations; onset of AGS symptoms is
often described in association with a febrile illness. Id. According to Dr. Barañano, H.H.’s clinical
presentation is entirely consistent with AGS and it is more likely that a genetic disorder like AGS
explains H.H.’s neurologic condition, rather than a molecular mimicry-like process triggered by
the vaccination. Id. It is Dr. Barañano’s opinion that H.H.’s clinical picture is consistent with AGS,
with his elevated liver enzymes, high CSF neopterin and biopterin levels, elevated interferon-alpha
levels in blood and CSF. Id. at 5-6.
In Dr. Barañano’s second report, she opined that normalized neopterin levels are reported
in 25% of AGS cases. Second Barañano Rep. at 1. The normalization of H.H.’s neopterin levels
does not provide support that this was a vaccine-mediated process. Id. It remains Dr. Barañano’s
opinion that H.H. falls into the 5% of AGS cases where a genetic marker has not been identified.
Id.
3. Testimony
Dr. Barañano provided a summary of AGS. Tr. at 253-54. When cells break down in our
body and release DNA products, such as nucleotides, the immune system is activated to clean up
the nucleotides. Id. at 253. In AGS, patients with the known AGS genes sense aberrant nucleotides
and attack its own body and nucleotides. Id. at 254. There are classical traits in AGS patients,
namely calcifications in the brain, white matter abnormalities, and skin lesions, however over time,
a greater spectrum of AGS phenotypes have been discovered, including children with later onset
and even some adult patients. Id. at 254-55. Dr. Barañano treats a number of AGS patients,
including one with a later onset. Id. at 255. AGS is generally an autosomal recessive gene; if H.H.’s
parents were carriers, there would be a 25% chance with each pregnancy of having an affected
child. Id. at 256.
Interferon alpha is not tested in the United States, so other doctors, like Dr. Crow, will run
the tests. Tr. at 261-62. Dr. Barañano’s understanding is that interferon alpha is “essentially
thought to be pathognomonic for AGS” meaning it goes hand in hand with the diagnosis of AGS.
Id. at 262. With more patients who are confirmed with the genetic markers for AGS, we have seen
more and more AGS phenotypes, thus calcifications are not considered mandatory for an AGS
diagnosis. Id. at 262-63.
Dr. Barañano discussed exhibit 83, a case study of children who have the confirmed gene
for AGS but do not have calcifications. Id. at 263. Dr. Barañano stated that a definite genetic
diagnosis only happens in 25-40% of cases. Id. at 264. Whole genome sequencing is a
breakthrough but “not the end all, be all.” Id. at 264. Dr. Barañano opined that she has not yet seen
a report regarding testing for the seventh AGS gene, and would have also recommended a
chromosomal microarray. Id. at 264-65. Dr. Barañano also stated that Dr. Vanderver’s research
program offers whole genome sequencing so her diagnostic rate is around 85%. Id. at 266. There
are improvements in genetic testing but there are still limitations. Id. Of 20,000 genes, only 5,000
are in the online Mendelian Inheritance in Man database. Id. at 267.
44
Dr. Barañano reiterated that H.H.’s onset at 15-16 months of age did not affect her opinion
that AGS is still the best clinical diagnosis at this time. Tr. at 268. H.H.’s irritability is consistent
with the onset of neurological symptoms. Id. The clinical course for AGS involves acute
neurologic symptoms followed by a period of stabilization. Dr. Barañano disagreed with Dr.
Marks’ assessment that AGS is a relentlessly progressive neurodegenerative disorder. Id. at 270.
Dr. Barañano added that the nervous system’s normal programming is to make developmental
progress, so if you superimpose a neurodegenerative process on that, a child plateaus and starts
losing skills, but if the disease has stabilized, a child’s underlying developmental process can
continue forward even though he remains severely impaired; thus improvement is not inconsistent
with AGS. Id. at 271.
Dr. Barañano confirmed that to the best of her knowledge there is no literature that
discusses the flu or Pentacel vaccines causing a Type 1 interferonopathy. Id. at 271-72. Dr.
Barañano also testified that other interferonopathies exist but AGS presents in the central nervous
system, affecting the brain, whereas other interferonopathies are more systemic. Id. at 273-74. Dr.
Barañano also stated that skin rashes were seen in 40% of AGS cases so it is not a universal finding.
Id. at 277. In short, there is nothing in H.H.’s presentation that is inconsistent with AGS. Id. at
293. However, without a genetic confirmation, Dr. Barañano cannot say definitively that H.H. has
AGS, just that it is the most likely diagnosis. Id. at 296.
V. Applicable Law
A. Petitioner’s Burden in Vaccine Program Cases
Under the Vaccine Act, when a petitioner suffers an alleged injury that is not listed in the
Vaccine Injury Table, a petitioner may demonstrate that he suffered an “off-Table” injury.
§ 11(c)(1)(C)(ii).
In attempting to establish entitlement to a Vaccine Program award of compensation for a
off-Table claim, a petitioner must satisfy all three of the elements established by the Federal Circuit
in Althen v. Sec’y of Health & Hum. Servs., 418 F.3d 1274 (Fed. Cir. 2005). Althen requires that
petitioner establish by preponderant evidence that the vaccination he received caused his injury
“by providing: (1) a medical theory causally connecting the vaccination and the injury; (2) a logical
sequence of cause and effect showing that the vaccination was the reason for the injury; and (3) a
showing of a proximate temporal relationship between vaccination and injury.” Id. at 1278.
Under the first prong of Althen, petitioners must provide a “reputable medical theory,”
demonstrating that the vaccine received can cause the type of injury alleged. Pafford, 451 F.3d at
1355-56 (citations omitted). To satisfy this prong, a petitioner’s theory must be based on a “sound
and reliable medical or scientific explanation.” Knudsen v. Sec’y of Health & Hum. Servs., 35 F.3d
543, 548 (Fed. Cir. 1994). Proof that the proffered medical theory is reasonable, plausible, or
possible does not satisfy a petitioner’s burden. Boatmon v. Sec’y of Health & Hum. Servs., 941
F.3d 1351, 1359-60 (Fed. Cir. Nov. 7, 2019).
Petitioners may satisfy the first Althen prong without resort to medical literature,
epidemiological studies, demonstration of a specific mechanism, or a generally accepted medical
45
theory. Andreu v. Sec’y of Health & Hum. Servs., 569 F.3d 1367, 1378-79 (Fed. Cir. 2009) (citing
Capizzano v. Sec’y of Health & Hum. Servs., 440 F.3d 1317, 1325-26 (Fed. Cir. 2006). However,
special masters are “entitled to require some indicia of reliability to support the assertion of the
expert witness.” Boatmon, 941 F.3d at 1360, quoting Moberly v. Sec’y of Health & Hum. Servs.,
592 F.3d 1315, 1324 (Fed. Cir. 2010). Special Masters, despite their expertise, are not empowered
by statute to conclusively resolve what are complex scientific and medical questions, and thus
scientific evidence offered to establish Althen prong one is viewed “not through the lens of the
laboratorian, but instead from the vantage point of the Vaccine Act’s preponderant evidence
standard.” Id. at 1380. Accordingly, special masters must take care not to increase the burden
placed on petitioners in offering a scientific theory linking vaccine to injury. Contreras v. Sec’y of
Health & Hum. Servs., 121 Fed. Cl. 230, 245 (2015), vacated on other grounds, 844 F.3d 1363
(Fed. Cir. 2017); see also Hock v. Sec’y of Health & Hum. Servs., No. 17-168V, 2020 U.S. Claims
LEXIS 2202 at *52 (Fed. Cl. Spec. Mstr. Sept. 30, 2020).
The second Althen prong requires proof of a logical sequence of cause and effect, usually
supported by facts derived from a petitioner’s medical records. Althen, 418 F.3d at 1278; Andreu,
569 F.3d at 1375-77; Capizzano, 440 F.3d at 1326 (“medical records and medical opinion
testimony are favored in vaccine cases, as treating physicians are likely to be in the best position
to determine whether a ‘logical sequence of cause-and-effect show[s] that the vaccination was the
reason for the injury’”) (quoting Althen, 418 F.3d at 1280). Medical records are generally viewed
as particularly trustworthy evidence, since they are created contemporaneously with the treatment
of the patient. Cucuras v. Sec’y of Health & Hum. Servs., 993 F.2d 1525, 1528 (Fed. Cir. 1993).
However, medical records and/or statements of a treating physician’s views do not per se
bind the special master to adopt the conclusions of such an individual, even if they must be
considered and carefully evaluated. Section 13(b)(1) (providing that “[a]ny such diagnosis,
conclusion, judgment, test result, report, or summary shall not be binding on the special master or
court”). As with expert testimony offered to establish a theory of causation, the opinions or
diagnoses of treating physicians are only as trustworthy as the reasonableness of their suppositions
or bases. The views of treating physicians should also be weighed against other, contrary evidence
also present in the record. Hibbard v. Sec’y of Health & Hum. Servs., 100 Fed. Cl. 742, 749 (2011),
aff’d, 698 F.3d 1355 (Fed. Cir. 2012); Caves v. Sec’y of Health & Hum. Servs., No. 06-522V, 2011
WL 1935813, at *17 (Fed. Cl. Spec. Mstr. Apr. 29, 2011), mot. for review den’d, 100 Fed. Cl. 344,
356 (2011), aff’d without opinion, 475 Fed. App’x 765 (Fed. Cir. 2012).
The third Althen prong requires establishing a “proximate temporal relationship” between
the vaccination and the injury alleged. Althen, 418 F.3d at 1281. That term has been equated to
the phrase “medically-acceptable temporal relationship.” Id. A petitioner must offer “preponderant
proof that the onset of symptoms occurred within a timeframe which, given the medical
understanding of the disorder’s etiology, it is medically acceptable to infer causation.” de Bazan
v. Sec’y of Health & Hum. Servs., 539 F.3d 1347, 1352 (Fed. Cir. 2008). The explanation for what
is a medically acceptable timeframe must also coincide with the theory of how the relevant vaccine
can cause an injury (Althen prong one’s requirement). Id. at 1352; Shapiro v. Sec’y of Health &
Hum. Servs., 101 Fed. Cl. 532, 542 (2011), recons. den’d after remand, 105 Fed. Cl. 353 (2012),
aff’d mem., 503 F. App’x 952 (Fed. Cir. 2013); Koehn v. Sec’y of Health & Hum. Servs., No. 11-
46
355V, 2013 WL 3214877 (Fed. Cl. Spec. Mstr. May 30, 2013), mot. for review den’d (Fed. Cl.
Dec. 3, 2013), aff’d, 773 F.3d 1239 (Fed. Cir. 2014).
The Vaccine Act defines significant aggravation as “any change for the worse in a
preexisting condition which results in markedly greater disability, pain, or illness accompanied by
substantial deterioration of health.” § 300aa-33(4). In Loving, the United States Court of Federal
Claims established the governing six-part test for off-Table significant aggravations. Petitioner
must prove by a preponderance of the evidence:
(1) The person’s condition prior to administration of the vaccine, (2) the person’s
current condition (or the condition following the vaccination if that is also
pertinent), (3) whether the person’s current condition constitutes a ‘significant
aggravation’ of the person’s condition prior to vaccination, (4) a medical theory
causally connecting such a significant worsened condition to the vaccination, (5) a
logical sequence of cause and effect showing that the vaccination was the reason
for the significant aggravation, and (6) a showing of a proximate temporal
relationship between the vaccination and the significant aggravation.
Loving v. Sec’y of Health & Hum. Servs., 86 Fed. Cl. 135, 144 (2009); see also W.C. v. Sec’y of
Health & Human Servs., 704 F.3d 1352, 1357 (Fed. Cir. 2013) (adopting this as the proper legal
standard for significant aggravation claims brought under the Vaccine Act). Loving prongs four,
five, and six are derived from the Federal Circuit’s test for off-Table actual causation cases. Althen
v. Sec’y of Health & Hum. Servs., 17 F.3d 374 (Fed. Cir. 1994).
In Sharpe, the Federal Circuit clarified the Loving prongs and what is required by
petitioners to successfully demonstrate a causation-in-fact significant aggravation claim. Sharpe
v. Sec’y of Health & Hum. Servs., 964 F.3d 1072 (Fed. Cir. 2020). Loving prong three only requires
a comparison of a petitioner’s current, post-vaccination condition with his pre-existing pre-
vaccination condition. Sharpe at 1082; Whitecotton v. Sec’y of Health & Hum. Servs., 81 F.3d
1099 (Fed. Cir. 1996). A petitioner is not required to demonstrate an expected outcome or that his
post-vaccination condition was worse than such an expected outcome. Sharpe at 1081. Further, a
petitioner is not required “to disprove tha
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