Overview
Dr. Pritchard is a Michigan native who returned to the University of Michigan to join the faculty here in 2019 after completing her pediatrics and genetics residencies and biochemical genetics fellowship. She enjoys care of complex patients with rare genetic diseases. Dr. Pritchard is active in medical education as Program Director for the Medical Biochemical Genetics Fellowship program and Associate Program Director for the Medical Genetics and Genomics training programs.Outside of work, Dr. Pritchard enjoys cooking, reading, hiking, and spending time with her husband and two daughters.
Dr. Pritchard is highly rated in 149 conditions, according to our data. Her clinical expertise encompasses Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Cockayne Syndrome Type 2.
She is actively involved in clinical research, co-authoring 14 peer reviewed articles.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- MANAGED MEDICAID PLAN
- OTHER COMMERCIAL
- HMO
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- POS
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
Locations
1540 E Hospital Dr, Floor 6 Reception C, Ann Arbor, MI 48109
1000 Wall St, Floor 1, Ann Arbor, MI 48105
Additional Areas of Focus
Dr. Pritchard has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
C. S. Mott Children's Hospital
Donna Martin is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Martin is highly rated in 1 condition, according to our data. Her clinical expertise encompasses CHARGE Syndrome and Neurofibromatosis Type 1 (NF1).
C. S. Mott Children's Hospital
Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ahmad is highly rated in 50 conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics.
C. S. Mott Children's Hospital
Mark Hannibal is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Hannibal is highly rated in 166 conditions, according to our data. His clinical expertise encompasses Aase Syndrome, Char Syndrome, DOOR Syndrome, and Cohen Syndrome. Dr. Hannibal is board certified in Clinical Genetics & Genomics.
Frequently Asked Questions about Dr. Amanda B. Pritchard
How do I make an appointment with Dr. Amanda B. Pritchard?
You can book an appointment with Dr. Amanda B. Pritchard by calling their office at 734-764-0579. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Amanda B. Pritchard a top-rated expert for Microcephaly Deafness Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Amanda B. Pritchard is classified as an Distinguished expert for Microcephaly Deafness Syndrome, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Amanda B. Pritchard specialize in?
While Dr. Amanda B. Pritchard is a Medical Genetics, they have specific expertise in Microcephaly Deafness Syndrome, Propionic Acidemia, and Delayed Growth. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Amanda B. Pritchard participate in research or clinical trials?
Yes. Dr. Amanda B. Pritchard has published 14 articles and abstracts on conditions like Microcephaly Deafness Syndrome. You can view a list of Dr. Amanda B. Pritchard's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Amanda B. Pritchard accept my insurance?
Dr. Amanda B. Pritchard accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 734-764-0579 to verify that your specific plan is currently accepted before your visit.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Distinguished
- Microcephaly Deafness SyndromeDr. Pritchard isDistinguished. Learn about Microcephaly Deafness Syndrome.
- Advanced
- 15q11.2 MicrodeletionDr. Pritchard isAdvanced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Pritchard isAdvanced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Pritchard isAdvanced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Pritchard isAdvanced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Pritchard isAdvanced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Pritchard isAdvanced. Learn about Aase Syndrome.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- AcrocephalopolydactylyDr. Pritchard isExperienced. Learn about Acrocephalopolydactyly.
- Acrofacial Dysostosis Rodriguez TypeDr. Pritchard isExperienced. Learn about Acrofacial Dysostosis Rodriguez Type.
- Acrofrontofacionasal Dysostosis SyndromeDr. Pritchard isExperienced. Learn about Acrofrontofacionasal Dysostosis Syndrome.
- Acromegaloid Facial Appearance SyndromeDr. Pritchard isExperienced. Learn about Acromegaloid Facial Appearance Syndrome.
- Activated PI3K Delta Syndrome (APDS)Dr. Pritchard isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).