Children's National Hospital
111 Michigan Ave NWWashington, DC, 20010
Andrea Gropman, M.D., is the Division Chief, Neurodevelopmental Pediatrics and Neurogenetics at Children's National Hospital. She specializes in neurogenetics, with a focus on mitochondrial disorders and Smith Magenis syndrome.
| Institution | Focus | Year |
|---|---|---|
| Residency - Johns Hopkins University Affiliated Hospitals | 1992 | |
| Continuing Medical Education (CME) - Post-doctoral, Genetics, Biochemical Genetics, National Institutes of Health, Human Genome Research Institute, Bethesda MD | 1997 | |
| Continuing Medical Education (CME) - George Washington University, Washington, DC, Psychiatry and Neurology | Neurology | Not Specified |
| Continuing Medical Education (CME) - National Institutes of Health Clinical Center, Bethesda, MD, Genetics, Clinical [General] | Not Specified | |
| Continuing Medical Education (CME) - Johns Hopkins University, Baltimore MD | Pediatrics | Not Specified |
| Continuing Medical Education (CME) - Children`s National Medical Center, Washington, DC, Psychiatry and Neurology w/sp Quals in Child Neur | Neurology | Not Specified |
| Fellowship - Neurology, George Washington University/Children's National Medical Center, Washington DC | 1994 |
| Certification | Cert. Body | Year |
|---|---|---|
| Clinical Biochemical Genetics | Medical Genetics | Not Specified |
| Clinical Genetics (MD) | Medical Genetics | Not Specified |
| Pediatrics | Pediatrics | Not Specified |
| Neurology with Special Qualification in Child Neurology Sub-Specialty: Neurodevelopmental Disabilities | Psychiatry and Neurology | Not Specified |
| Pediatrics | Dermatology | Not Specified |
| Role | Organization | Time |
|---|---|---|
| Member | Center for Neuroscience Research | Present |
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Accepts New Patients: Yes
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