Markus Grompe, M.D.
- Special Interest:
- Metabolic Diseases
- Accepting Patients:
- English, German
Dr. Grompe is involved in the clinical care of patients with genetic diseases, especially inborn errors of metabolism such as phenylketonuria. He is experienced at diagnosing and managing disorders of amino acid metabolism, organic acidurias, urea cycle disorders, lysosomal storage disorders and carbohydrate metabolism disorders. His special interest is in genetic conditions that cause hepatic dysfunction, for example glycogen storage diseases.
M.D., University of Ulm Medical School, Germany, 1983
Oregon Health & Science University, Portland
Medical Genetics, Baylor College of Medicine, Houston, TX, 1991
Biochemical Genetics, Baylor College of Medicine, Houston, TX, 1991
American Board of Pediatrics, 1989.
American Board of Human Genetics, 1990.