The 20 Best Propionic Acidemia Doctors in The United States

Charles Venditti is a Medical Genetics provider practicing medicine in Bethesda, Maryland. Dr. Venditti is rated as an Elite provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 8 other conditions, according to our data. His clinical expertise encompasses Methylmalonic Acidemia, Propionic Acidemia, Homocystinuria, and Niemann-Pick Disease.

Oleg Shchelochkov is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Iowa City, Iowa. Dr. Shchelochkov is rated as an Elite provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Propionic Acidemia, Argininosuccinic Aciduria, Methylmalonic Acidemia, and Urea Cycle Disorders (UCD).

Susan Berry is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Minneapolis, Minnesota. Dr. Berry is rated as a Distinguished provider by MediFind in the treatment of Propionic Acidemia. She is also highly rated in 23 other conditions, according to our data. Her clinical expertise encompasses Urea Cycle Disorders (UCD), Propionic Acidemia, Argininosuccinic Aciduria, and Inborn Amino Acid Metabolism Disorder. Dr. Berry is board certified in Clinical Genetics And Genomics: American Board Of Medical Genetics And Genomics, 1984 and Pediatrics: American Board Of Pediatrics, 1983. Dr. Berry is currently accepting new patients.

Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ahmad is rated as a Distinguished provider by MediFind in the treatment of Propionic Acidemia. She is also highly rated in 50 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics.

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 Propionic Acidemia. She is also highly rated in 12 other conditions, according to our data. Her clinical expertise encompasses Methylmalonic Acidemia, Propionic Acidemia, Progressive External Ophthalmoplegia, and Infantile Neutropenia. Dr. Vernon is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Nicholas Ah Mew, MD, is director of the Inherited Metabolic Disorders Program at Children’s National Hospital and is associate professor of Pediatrics at The George Washington University. He is a clinical geneticist and clinical biochemical geneticist whose primary research interests include urea cycle disorders, organic acidemias, and other disorders of ammonia metabolism. He is the principal investigator or co-PI of several projects funded through the National Institutes of Health and Patient-Centered Outcomes Research Institute. Dr. Ah Mew is the Children’s National site-PI and an active member of the NIH-funded Urea Cycle Disorders Consortium (UCDC). He has authored multiple publications and book chapters on hyperammonemia and urea cycle disorders and has lectured internationally on these topics. Dr. Mew is rated as a Distinguished provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Maple Syrup Urine Disease, Argininosuccinic Aciduria, and Propionic Acidemia. Dr. Mew is board certified in American Board Of Medical Genetics And Genomics, 2020 and Clinical Biochemical Genetics: American Board Of Medical Genetics And Genomics, 2011.

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 an Advanced provider by MediFind in the treatment of Propionic Acidemia. She is also highly rated in 27 other conditions, according to our data. Her clinical expertise encompasses Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation. Dr. Hamosh is board certified in American Board Of Medical Genetics And Genomics.

Anthony Perszyk is a Medical Genetics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Perszyk is rated as an Experienced provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Mucolipidosis 3. Dr. Perszyk is board certified in American Board Of Medical Genetics And Genomics.

Gregory Enns is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Palo Alto, California. Dr. Enns is rated as a Distinguished provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 52 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Methylmalonic Acidemia, Arginase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Dr. Enns is currently accepting new patients.

Marshall Summar is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Chevy Chase, Maryland. Dr. Summar is rated as a Distinguished provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Argininosuccinic Aciduria, Urea Cycle Disorders (UCD), Propionic Acidemia, and Ornithine Translocase Deficiency.

Joel Charrow is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Chicago, Illinois. Dr. Charrow is rated as a Distinguished provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 45 other conditions, according to our data. His clinical expertise encompasses Gaucher Disease Type 1, Gaucher Disease, Achondroplasia, Isovaleric Acidemia, and Splenectomy.

Vernon Sutton is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Austin, Texas. Dr. Sutton is rated as a Distinguished provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 31 other conditions, according to our data. His clinical expertise encompasses Osteogenesis Imperfecta, Robinow Syndrome, Genital Dwarfism, and 2q37 Deletion Syndrome. Dr. Sutton is currently accepting new patients.

Rebecca Mardach is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Los Angeles, California. Dr. Mardach is rated as a Distinguished provider by MediFind in the treatment of Propionic Acidemia. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Gaucher Disease Type 1, Gaucher Disease, Propionic Acidemia, and Farber Lipogranulomatosis.

Joshua Baker is a Pediatrics provider practicing medicine in Chicago, Illinois. Dr. Baker is rated as a Distinguished provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 152 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Acid Sphingomyelinase Deficiency (ASMD), and Propionic Acidemia.

Richard Chang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Chang is rated as an Advanced provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 155 other conditions, according to our data. His clinical expertise encompasses Citrullinemia, Beta-Ketothiolase Deficiency, Biotinidase Deficiency, and Adrenoleukodystrophy (ALD). Dr. Chang is currently accepting new patients.

David Sweetser is a Pediatrics provider practicing medicine in Boston, Massachusetts. Dr. Sweetser is rated as an Advanced provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Hypotonia, Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, and Propionic Acidemia. Dr. Sweetser is board certified in Pediatrics, Clinical Biochemical Genetics, Pediatric Hematology-Oncology, and Clinical Genetics And Genomics.

Jose Abdenur is a Medical Genetics provider practicing medicine in Orange, California. Dr. Abdenur is rated as an Advanced provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 41 other conditions, according to our data. His clinical expertise encompasses Glycogen Storage Disease Type 9, Von Gierke Disease, Glycogen Storage Disease Type 3, and Malonyl-CoA Decarboxylase Deficiency. Dr. Abdenur is currently accepting new patients.

Amy Kritzer is a Pediatrics provider practicing medicine in Boston, Massachusetts. Dr. Kritzer is rated as an Advanced provider by MediFind in the treatment of Propionic Acidemia. She is also highly rated in 33 other conditions, according to our data. Her clinical expertise encompasses Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Biotinidase Deficiency, and Smith-Lemli-Opitz Syndrome. Dr. Kritzer is board certified in Pediatrics, Medical Biochemical Genetics, and Clinical Genetics And Genomics.

Richard Schroer is a Medical Genetics provider practicing medicine in Charleston, South Carolina. Dr. Schroer is rated as an Experienced provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Chromosome 2p Duplication, Propionic Acidemia, Phenylketonuria (PKU), and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Dr. Schroer is currently accepting new patients.

Dr. Changrui Xiao is a board-certified UCI Health neurologist, clinical geneticist and medical biochemical geneticist who specializes in neurogenetic and inherited metabolic disorders.His clinical interests include lysosomal storage diseases, hereditary and spinocerebellar ataxia, neurometabolic disorders, inborn errors of metabolism in adults, late onset Tay-Sachs and Sandhoff diseases, and genomic diagnosis.Xiao earned his medical degree at Duke University School of Medicine in Durham, N.C. He completed an internship in internal medicine and a residency in neurology at the University of Chicago Medical Center in Illinois. He received fellowship training in medical genetics and medical biochemical genetics at the National Institutes of Health Clinical Center and Johns Hopkins Hospital in Bethesda, Md., and Children's National Hospital in Washington, D.C. Before joining UCI Health, he was a clinician with the National Institutes of Health Undiagnosed Disease Program.He is the author or co-author of numerous peer-reviewed publications and presentations. He is an associate editor of the journalMolecular Genetics & Genomic Medicineand a consulting editor forGeneReviews. His goal is to provide a medical home for adults with neurogenetic and metabolic conditions, and to increase access to precision therapy for these conditions. Dr. Xiao is rated as an Experienced provider by MediFind in the treatment of Propionic Acidemia. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Retinopathy Pigmentary Mental Retardation, Glutaric Acidemia Type 2, Adrenoleukodystrophy (ALD), and X-Linked Creatine Deficiency. Dr. Xiao is board certified in American Board Of Medical Genetics And Genomics - Clinical Genetics And Genomics and American Board Of Psychiatry And Neurology - Neurology.