Markus Grompe, M.D.

Academic and Clinical Positions

Member, Division of Biochemical Genetics

Professor

Biography

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.

Professional Education

• Degree:
  M.D., University of Ulm Medical School, Germany, 1983
  
• Residency:
  Oregon Health & Science University, Portland
• Fellowships:
  Medical Genetics, Baylor College of Medicine, Houston, TX, 1991
  Biochemical Genetics, Baylor College of Medicine, Houston, TX, 1991
  

Certifications

• Certifications:
  American Board of Pediatrics, 1989.
  American Board of Human Genetics, 1990.
  

Memberships and Associations

American Board of Human Genetics , American Society for Gene Therapy, International Society for Stem Cell Research, Society for Pediatric Research