Dr. Amanda Barone Pritchard is an Assistant Professor of Pediatrics at University of Michigan Health in the division of Pediatric Genetics, Metabolism, and Genomic Medicine. Dr. Pritchard attended the University of Pittsburgh School of Medicine before completing Pediatric Residency at Lurie Children’s Hospital in Chicago. She then trained in Medical Genetics and Genomics and completed a Medical Biochemical Genetics fellowship at the Children’s Hospital of Philadelphia. She currently practices pediatric genetics and biochemical genetics, and has research interests in delineation of new genetic disorders and treatment of genetic diseases. She has been involved in several clinical trials for inborn errors of metabolism. Dr. Pritchard is also an enthusiastic medical educator and serves as Program Director for the Medical Biochemical Genetics Fellowship and Associate Program Director for the Medical Genetics and Genomics and Combined Pediatrics-Medical Genetics and Genomics Residency Programs at the University of Michigan.