Harvey Levy, MD
Dr. Harvey Levy is Senior Physician in Medicine/Genetics at Boston Children’s Hospital and Professor of Pediatrics at Harvard Medical School. He has devoted his career of 50 years to the diagnosis, research, and treatment of metabolic disorders.
Following graduation from the Medical College of Georgia Dr. Levy trained in pediatrics in Boston, New York, and Baltimore. Following pediatric training, Dr. Levy then served a fellowship in metabolic disorders at the Massachusetts General Hospital (MGH) under Dr. Mary Efron, a pioneer in metabolism. After completing this training, Dr. Levy joined the faculty of the MGH and Harvard and also served as Consultant in Metabolism to the Massachusetts Newborn Screening Program. In 1978, Dr. Levy moved to Boston Children’s Hospital to found and serve as Director of the Metabolic Program, now the Biochemical Genetics section of the Division of Genetics.
Dr. Levy developed a specific interest in Homocystinuria during his fellowship when he identified the first case diagnosed from newborn screening. Shortly thereafter he and Dr. Harvey Mudd discovered the first example of increased homocysteine due to a non-homocystinuric disorder, now known as cobalamin C defect. This was also the first example of a human disorder of vitamin B12 metabolism. Disorders of sulfur metabolism have continued to be a major interest of Dr. Levy throughout his career. He has authored over 400 medical articles and book chapters on metabolic disorders, including many on the homocystinemias, and has received a number of national and international awards for his achievements.