Amanda Barone Pritchard, MD

Amanda Barone Pritchard, MD

Specialty: Clinical Genetics, Pediatrics
Title: Clinical Associate Professor
4.7/5
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Amanda Barone Pritchard, MD
Amanda Barone Pritchard, MD
Clinical Genetics
  • About
  • Areas of Practice
  • Locations
  • Insurance
  • Education & Training
  • Research Overview
  • Patient Ratings & Comments
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  • About

    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.

    Areas of Practice

    pediatric genetics, medical biochemical genetics, ophthalmic genetics, lysosomal storage diseases, newborn screening follow-up

    Locations

    • Pediatric Genetics Clinic | C. S. Mott Children's Hospital 1540 E Hospital Dr
      Floor 6 Reception C
      Ann Arbor, MI 48109-4234
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    • Pediatric Ophthalmology & Adult Strabismus Clinic | Kellogg Eye Center 1000 Wall St
      Floor 1
      Ann Arbor, MI 48105-1912
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    • Craniofacial & Plastic Surgery Clinic | C. S. Mott Children's Hospital 1540 E Hospital Dr
      Floor 3 Reception B
      Ann Arbor, MI 48109-4219
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    Insurance Accepted

    University of Michigan Health participates with most health insurance plans.

    See our insurance details

    Education & Training

    Medical School or Training

    University of Pittsburgh, 2013

    Residency

    Children's Memorial Hospital (Lurie Children's Hospital of Chicago), Pediatrics, 2016
    Children's Hospital of Philadelphia, Medical Genetics, 2017
    Children Hospital of Philadelphia, Medical Genetics, 2017
    Children Memorial Hospital (Lurie Children Hospital of Chicago), Pediatrics, 2016

    Fellowships

    Children's Hospital of Philadelphia, Medical & Biochemical Genetics, 2018
    Children Hospital of Philadelphia, Medical & Biochemical Genetics, 2018

    Board Certifications

    Pediatrics
    Clinical Genetics & Genomics
    Medical Biochemical Genetics

    Professional Organizations

    American Academy of Pediatrics
    American College of Medical Genetics and Genomics
    Association of Professors of Human and Medical Genetics
    Society for Inherited Metabolic Disorders

    Research Overview

    Dr. Pritchard's research interests include newborn screening, treatment of genetic diseases, clinical trials, ophthalmic genetics, medical education in genetics, and delineation of newly recognized genetic syndromes.

    Patient Ratings & Comments

    Visit our Physician Ratings & Comments page to learn more about how patient ratings are collected, calculated, and updated to help you make an informed decision when choosing the right physician for your care.

    Patient Ratings

    31 Patient Ratings

    Patient Comments

    July 24, 2025 - "Dr. Pritchard was kind, thorough, and extremely knowledgeable. She took the time to explain things and answer all questions."

    June 17, 2025 - "[...] and Dr. Pritchard were absolutely incredible. They listened intently, gave information in a way that was understandable, and clearly explained our options. I'm very grateful for their help. [...]"

    June 7, 2025 - "We see Dr. Pritchard to treat our son's [...] disorder. While we're pretty well-educated parents, genetics and biochemistry aren't easy to understand. I am always impressed by the way Dr Pritchard explains material. It's easy to understand, provides aha moments when different information connects, makes us feel confident as parents, and allays our fears."