Amanda B. Pritchard
Expertise in
150
conditions

Dr. Amanda B. Pritchard

Medical Genetics | Pediatrics
University Of Michigan Pediatric Genetics Clinic
1540 East Hospital Drive, Floor 6, 
Ann Arbor, MI 
Accepting New Patients
Expertise in
150
conditions
University Of Michigan Pediatric Genetics Clinic
1540 East Hospital Drive, Floor 6, 
Ann Arbor, MI 

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 150 conditions, according to our data. Her clinical expertise encompasses Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Costello Syndrome.

Dr. Pritchard is board certified in American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2019 , American Board Of Pediatrics, Pediatrics - 2016, and American Board Of Medical Genetics And Genomics, Medical Biochemical Genetics - 2019 . She is actively involved in clinical research, co-authoring 16 peer reviewed articles. Dr. Pritchard is currently accepting new patients.

Specialties

Medical Genetics
Pediatrics

Licenses

Pediatrics in MI

Board Certifications

American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2019
American Board Of Pediatrics, Pediatrics - 2016
American Board Of Medical Genetics And Genomics, Medical Biochemical Genetics - 2019

Hospital Affiliations

University Of Michigan Health System

Languages Spoken

English

Gender

Female

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Aetna
  • EPO
  • HMO
  • POS
  • PPO
Anthem BCBS
  • EPO
  • HMO
  • POS
  • PPO
Blue Cross Blue Shield
  • EPO
  • HMO
  • POS
  • PPO
Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO
Managed Health Services
  • EPO
  • MANAGED MEDICAID PLAN
  • OTHER COMMERCIAL
McLaren Health
  • HMO
Medicaid
  • OTHER MEDICAID
  • STATE MEDICAID
Priority Health
  • HMO
  • POS
Spectrum Priority Health
  • HMO
  • INSURANCE PLAN
  • MANAGED MEDICAID PLAN
  • MEDICARE MAPD
  • MEDICARE PDP
  • OTHER COMMERCIAL
View 4 Less Insurance Carriers -

Locations

University of Michigan Pediatric Genetics Clinic
1540 East Hospital Drive, Floor 6, Ann Arbor, MI 48109
Other Locations
Pediatric Ophthalmology & Adult Strabismus Clinic
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.

Neurofibromatosis Type 1 (NF1)

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.

16 Total Publications

Phenotype variability in six new patients with beta-mannosidosis.
Phenotype variability in six new patients with beta-mannosidosis.
Journal: Molecular genetics and metabolism
Published: May 11, 2026
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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 16 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.

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