Andrea Gropman, MD Division Chief, Neurodevelopmental Disabilities and Neurogenetics


Languages Spoken

  • English


Board Certifications

  • American Board of Pediatrics
  • American Brd of Med Genetics/Clin Biochemical Gen
  • American Board of Psychiatry/Neurology-Child Neuro
  • American Board of Med. Genetics/Clinical Genetics
  • American Board of Ped/Neurodevelop. Disabilities


Andrea Gropman, MD, specializes in neurogenetics, with a focus on mitochondrial disorders and Smith Magenis syndrome.

Education & Training

Education & Training

  • MD, 1992
    University of Massachusetts Medical School
  • BA, Biology, 1986
    Brandeis University
Patient Stories

Patient Stories: Andrea Gropman, MD

Patient story

Johnathan M.'s Story

"We are blessed that we live so close to a wonderful facility that caters to children."



Research & Publications

Research & Publications

Fabry Patient Advisory Panel

(2006) The Genetics of Fabry Disease, Implications for Female Carriers

Childhood Mitochondrial Disorders and Other Inborn Errors of Metabolism Presenting with White Matter Disease

(2005) Bioimaging in Neurodegeneration

Atypical Patterns of Inheritance

(2007) Seminars in Pediatric Neurology

Developments in SmithMagenis Syndrome

(2007) Current Opinions in Neurology

National Urea Cycle Disease Foundation

(2007) The New Horizon: Studying the Effects of UCDs on Brain Function

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Austin's Story

Patient story

"People always tell me 'You're so strong, I don't know how you got through it.' I like to say that you never know how strong you are or what you are capable of until you have no choice but to be strong." 

Read More of Austin's Story