Charles Venditti is a Medical Genetics provider in Bethesda, Maryland. Dr. Venditti is rated as an Elite provider by MediFind in the treatment of Methylmalonic Acidemia. His top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Homocystinuria, and Niemann-Pick Disease.

Dr. Hilary Vernon is a Professor of Genetic Medicine and pediatrics at the Johns Hopkins University School of Medicine. She is also an attending physician at Kennedy Krieger Institute. Hilary Vernon has expertise in treating inborn errors of metabolism and mitochondrial disorders. She is the director of the Mitochondrial Care Center at The Johns Hopkins Hospital and the Barth Syndrome Interdisciplinary Clinic at the Kennedy Krieger Institute. Her research interests include understanding intermediary metabolism in Barth syndrome and in disorders of branch chain amino acid metabolism. Dr. Vernon also co-directs the Department of Genetic Medicine Clinical Trials Unit, and is the principal investigator on multiple clinical trials for rare diseases. Dr. Vernon received her medical degree and doctorate from Rutgers University, New Brunswick, New Jersey. She completed residencies in genetics and pediatrics at The Johns Hopkins University, and a fellowship in clinical laboratory biochemical genetics at The Johns Hopkins University. Dr. Vernon was recognized with the 2010 Francis F. Schwentker Award for Excellence in Research at Johns Hopkins University and the 2011 James B. Sidbury Jr. Fellowship in Biochemical Genetics at Johns Hopkins University. Dr. Vernon is rated as a Distinguished provider by MediFind in the treatment of Methylmalonic Acidemia. Her top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Infantile Neutropenia, Progressive External Ophthalmoplegia, and Gastrostomy.

Dr. Ada Hamosh is the Dr. Frank V. Sutland Professor of Pediatric Genetics in the Departments of Genetic Medicine and Pediatrics. Since 2002, she has served as clinical director of the McKusick-Nathans Institute of Genetic Medicine, now Department of Genetic Medicine and scientific director of the Online Mendelian Inheritance in Man® (OMIM), a catalog of more than 16,800 human genes and genetic disorders created by Dr. Victor A. McKusick. Her research centers the molecular basis of Mendelian disorders, the integration of genetics into clinical practice and the diagnosis and management of inborn errors of metabolism. Dr. Hamosh earned a bachelor’s degree in biology from Wesleyan University, a medical degree from Georgetown University School of Medicine and a master’s of public health from Johns Hopkins University School of Public Health. She later completed a fellowship in medical and biochemical genetics from the Johns Hopkins School of Medicine, before joining the Johns Hopkins faculty in 1992. Dr. Hamosh began her genetics career focusing on cystic fibrosis, serving as coordinator of the International Cystic Fibrosis Genotype-Phenotype Consortium. She served as chair of the Maryland State Advisory Council for Hereditary & Congenital Disorders from 2001-2009, during which time she also served on the executive committee of the Genetic Counseling Training Program, run by Johns Hopkins University and the National Human Genome Research Institute. Dr. Hamosh has authored more than 128 publications on a variety of topics. In addition, she is a member of 16 professional associations and advisory committees including the American Society of Human Genetics, the Steering Committee of the Global Alliance for Genomics and Health, and the executive board of the Human Genome Organization, of which she will be President from 2023-2025. Dr. Hamosh was recognized in Baltimore magazine as one of the region’s top doctors in 2013, and 2016-2020. Dr. Hamosh is rated as a Distinguished provider by MediFind in the treatment of Methylmalonic Acidemia. Her top areas of expertise are Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation.

Marshall Summar is a Medical Genetics specialist and a Pediatrics provider in Chevy Chase, Maryland. Dr. Summar is rated as an Advanced provider by MediFind in the treatment of Methylmalonic Acidemia. His top areas of expertise are Argininosuccinic Aciduria, Urea Cycle Disorders (UCD), Propionic Acidemia, and Ornithine Translocase Deficiency.

Robert Rapp is a primary care provider, practicing in Internal Medicine in Forest Hill, Maryland. Dr. Rapp is rated as an Advanced provider by MediFind in the treatment of Methylmalonic Acidemia. His top areas of expertise are Lung Metastases, Type 2 Diabetes (T2D), Methylmalonyl Coenzyme A Mutase Deficiency, and Methylmalonic Acidemia. Dr. Rapp is currently accepting new patients.

Gerard Champaloux is a primary care provider, practicing in Family Medicine in Bowie, Maryland. Dr. Champaloux is rated as an Advanced provider by MediFind in the treatment of Methylmalonic Acidemia. His top areas of expertise are Beta-Ketothiolase Deficiency, Methylmalonyl Coenzyme A Mutase Deficiency, Methylmalonic Acidemia, and Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease.

William Queale is a primary care provider, practicing in Internal Medicine in Forest Hill, Maryland. Dr. Queale is rated as an Advanced provider by MediFind in the treatment of Methylmalonic Acidemia. His top areas of expertise are Methylmalonic Acidemia, Methylmalonyl Coenzyme A Mutase Deficiency, Methylmalonic Acidemia with Homocystinuria, and Homocystinuria.

Constantine Stratakis is a Medical Genetics specialist and a Gastroenterologist in Bethesda, Maryland. Dr. Stratakis is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia. His top areas of expertise are Cushing's disease, Neuroendocrine Tumor, Gastrointestinal Stromal Tumor, Orchiectomy, and Hormone Replacement Therapy (HRT).

Nancy Braverman is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Braverman is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia. Her top areas of expertise are Zellweger Syndrome, Chondrodysplasia Punctata Syndrome, X-Linked Chondrodysplasia Punctata 2, and Acromesomelic Dysplasia.

Robin Wilson is a Neurologist in Baltimore, Maryland. Dr. Wilson is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia. Her top areas of expertise are Normal Pressure Hydrocephalus, Hydrocephalus, Congenital Cardiovascular Shunt, and Cerebellum Agenesis Hydrocephaly. Dr. Wilson is currently accepting new patients.

Dr. Sara Mixter is Assistant Professor of Medicine and Pediatrics at the Johns Hopkins University School of Medicine. Her areas of clinical expertise are internal medicine, pediatrics, and primary care for adults with developmental disabilities and other complex childhood-onset conditions. She is the director of the Hopkins PACT (Pediatric-informed Adult Care and Transition) Clinic. Dr. Mixter is also the medical director of the Pediatric Complex Care Collaborative (PC3) for the Johns Hopkins Children’s Center. Dr. Mixter received her A.B. from Harvard College. She earned her M.D. from Harvard Medical School and M.P.H. from the Harvard School of Public Health. She completed her residency at Johns Hopkins as part of the inaugural group of trainees in the Urban Health Combined Internal Medicine-Pediatrics Residency Program. Her research interests include transitions of care for adolescents with special healthcare needs and education for residents and medical students, especially in primary care and complex care. Dr. Mixter has served as the Assistant Chief of Service for the Longcope firm of the Osler Medical Housestaff Training Program (2015-16), as well as Assistant Program Director for Ambulatory Education (2014-15). Dr. Mixter is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia. Her top areas of expertise are Cerebral Palsy, Gastroparesis, Orbital Cellulitis, and Sickle Cell Disease.

Sofia Saenz-Ayala is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Saenz-Ayala is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia. Her top areas of expertise are Musculocontractural Ehlers-Danlos Syndrome (mcEDS), Ehlers-Danlos Syndrome (EDS), Carnitine Palmitoyltransferase 1 Deficiency, and Carnitine Palmitoyltransferase 2 Deficiency. Dr. Saenz-Ayala is currently accepting new patients.

Hans Bjornsson is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Bjornsson is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia. His top areas of expertise are Kabuki Syndrome, Weaver Syndrome, 3MC Syndrome, Coffin-Lowry Syndrome, and Orchiectomy. Dr. Bjornsson is currently accepting new patients.

Lisa Kratz is a Medical Genetics provider in Baltimore, Maryland. Dr. Kratz is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia. Her top areas of expertise are Greenberg Dysplasia, Smith-Lemli-Opitz Syndrome, Rhizomelic Syndrome, and Chondrodysplasia Punctata Syndrome.

Peter Mcguire is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Mcguire is rated as an Experienced provider by MediFind in the treatment of Methylmalonic Acidemia. His top areas of expertise are Ornithine Transcarbamylase Deficiency, Urea Cycle Disorders (UCD), Coenzyme Q Cytochrome C Reductase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.