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Advanced Training in Medical Biochemical Genetics

Welcome to the Medical Biochemical Genetics Fellowship Program at Case Western Reserve University / University Hospitals Cleveland Medical Center. Thank you for your interest in our program. Our mission is to provide top-notch advanced training to all of our fellows. Our education includes how to approach, diagnose, and potentially treat common and uncommon anomalies and syndromes. As each trainee is unique, individual training experiences are tailored as much as possible to each fellow’s areas of interest and career goals.

The Medical Biochemical Genetics Fellowship Program is a 1 year training program that emphasizes care and management of patients with inborn errors of metabolism. Trainees spend time in both the care of patients and the laboratory for learning about diagnostics related to metabolic disorders.

Fellows learn from 10 clinical genetics faculty with diverse training backgrounds that include neurology, urology, internal medicine, pediatrics and metabolic genetics. The majority of the clinical training occurs at UH Rainbow Babies & Children’s Hospital and University Hospitals. Fellows have the opportunity to attend many specialty and multidisciplinary clinics with one of our genetics faculty. Some of those clinics include Prader Willi clinic, Marfan Syndrome Clinic, Congenital Cardiac Malformations Clinic, Neurogenetics Clinic, Vascular Anomalies clinic, and Craniofacial clinic.

For More Information

For specific questions or additional information, please contact Marie Hoyle.

Marie Hoyle, BA
Program Coordinator

Mailing Address
Center for Human Genetics
Medical Genetics Residency Program
11100 Euclid Avenue
Lakeside 1500, First Floor
Cleveland, OH 44106

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