Dr. Uta Lichter-Konecki

RaeLynn Forsyth, MD, specializes in medical genetics as well as pediatric genetics and genomics and is board-certified by the American Board of Pediatrics and the American Board of Medical Genetics and Genomics. She practices at Medical Genetics Metabolic in Lawrenceville, Medical Genetics in Lawrenceville, and Medical Genetics in Erie and is affiliated with UPMC Hamot, UPMC Children's Hospital of Pittsburgh, UPMC Magee-Womens Hospital, and UPMC Presbyterian. Dr. Forsyth completed her medical degree and a fellowship at the University of Pittsburgh School of Medicine in addition to a residency and fellowship at The Johns Hopkins University School of Medicine. Dr. Forsyth is rated as an Advanced provider by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. Her top areas of expertise are Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Inborn Amino Acid Metabolism Disorder, and Carbamoyl Phosphate Synthetase 1 Deficiency.

Gerard (Jerry) Vockley MD, PhD, is a medical geneticist and is certified in clinical genetics and biochemical and molecular genetics by the American Board of Medical Genetics and Genomics. He is chief of the Division of Medical Genetics, director of the Center for Rare Disease Therapy, and is the Cleveland Family Endowed Professor of pediatric research at the University of Pittsburgh School of Medicine. He completed his medical degree and PhD at the University of Pennsylvania and completed his residency at the University of Colorado, followed by his fellowship at Yale University School of Medicine. Dr. Vockley is rated as an Advanced provider by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. His top areas of expertise are Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, and Arginase Deficiency.

Michael Trotta is a primary care provider, practicing in Pediatrics and Internal Medicine in Butler, Pennsylvania. Dr. Trotta is rated as an Advanced provider by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. His top areas of expertise are Infant Hyperglycemia, High Cholesterol, Vitamin D Deficiency, and Severe Fever with Thrombocytopenia Syndrome.