Dr. Amanda B. Pritchard
Overview
Amanda Pritchard is a Medical Genetics provider in Traverse City, Michigan. Dr. Pritchard has been practicing medicine for over 13 years is highly rated in 149 conditions, according to our data. Her top areas of expertise are Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Aase Syndrome. Dr. Pritchard is currently accepting new patients.
Her clinical research consists of co-authoring 12 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Graduate Institution
Residency
Specialties
Licenses
Board Certifications
Fellowships
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
106 South Madison Street, Traverse City, MI 49684
1540 East Hospital Drive, Floor 6, Ann Arbor, MI 48109
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.
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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 231-935-8125. 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 12 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 231-935-8125 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).