The 20 Best Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency Doctors in The United States
Find the Top Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency Experts and Specialists
Washington University
Peter Crawford is a Cardiologist practicing medicine in Saint Louis, Missouri. Dr. Crawford is rated as a Distinguished provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Heart Failure, and Hereditary Ataxia.
St. Christopher's Pediatric Associates Genetics - E. Erie Avenue
. Dr. Perszyk is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Mucolipidosis 3. Dr. Perszyk is board certified in American Board Of Medical Genetics And Genomics.
Medical Genetics Metabolic In Lawrenceville
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 Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, and Arginase Deficiency. Dr. Vockley is board certified in American Board Of Medical Genetics And Genomics and American Board Of Medical Genetics And Genomics.
C. S. Mott Children's Hospital
David Bradley is a Pediatrics specialist and a Pediatric Cardiologist practicing medicine in Ann Arbor, Michigan. Dr. Bradley is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 30 other conditions, according to our data. His clinical expertise encompasses Transposition of the Great Arteries, Tetralogy of Fallot, Congenital Heart Block, and Hypoplastic Left Heart Syndrome (HLHS).
Office
Joseph Risko is a primary care provider, practicing in Internal Medicine in Tavares, Florida. Dr. Risko is rated as a Distinguished provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 19 other conditions, according to our data. His clinical expertise encompasses Necrosis, Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Hypertensive Heart Disease, Colonoscopy, and Pacemaker Implantation.
Mt Endocrinology PC
Maggie Tavdy is an Endocrinologist practicing medicine in Yonkers, New York. Dr. Tavdy is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 19 other conditions, according to our data. Her clinical expertise encompasses Thyroid Nodule, Maturity Onset Diabetes of the Young, Type 2 Diabetes (T2D), and Hypothyroidism.
UT Southwestern - Pediatrics
Luis Umana is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Dallas, Texas. Dr. Umana is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 177 other conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Biotinidase Deficiency, and Argininosuccinic Aciduria.
Cristel Chapel is a Medical Genetics provider practicing medicine in Orange, California. Dr. Chapel is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses CLN4 Disease, CLN2 Disease, CLN3 Disease, and CLN5 Disease. Dr. Chapel is currently accepting new patients.
Vanderbilt University
Jenna Essakow is a Pediatrics provider practicing medicine in Nashville, Tennessee. Dr. Essakow is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency.
Sentara Pulmonary, Critical Care & Sleep Specialists
Michael Hooper is an Emergency Medicine provider practicing medicine in Norfolk, Virginia. Dr. Hooper is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Pulmonary Veno-Occlusive Disease, Pulmonary Hypertension, Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Cystic Fibrosis, and Endoscopy.
Connecticut Children's
Richard Pierce is a Pediatrics provider practicing medicine in Hartford, Connecticut. Dr. Pierce is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency and Multisystem Inflammatory Syndrome in Children (MIS-C).
C. S. Mott Children's Hospital
David Olson earned his M.D. and Ph.D. at the University of Michigan (the latter in Cellular and Molecular Biology). He served his internship and residency at Children’s Hospital Boston, followed by a fellowship in pediatric endocrinology and metabolism at Children’s Hospital Boston/Joslin Diabetes Center. Prior to returning to the University of Michigan, Dr. Olson was on staff at Children's Hospital Boston and affiliated with the Department of Newborn Medicine at Brigham and Women’s Hospital. His postdoctoral research was performed at Beth Israel Deaconess Medical Center, Division of Endocrinology. Using novel mouse models, Dr. Olson is exploring gene expression changes in specific neuronal populations in the brain that are known to be important in regulating energy balance; these studies are directed at examining the link between gene expression in specific areas of the brain and altered metabolism. Additional studies using neuron-specific genetic changes are underway to clarify the molecular basis of daily biologic rhythms and explore how disruption of these rhythms predisposes organisms (rodents and humans) to pathologic changes in metabolism. Dr. Olson is rated as an Experienced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 8 other conditions, according to our data. His clinical expertise encompasses Type 1 Diabetes (T1D), Short Stature (Growth Disorders), Idiopathic Short Stature (ISS), and Familial Short Stature (FSS). Dr. Olson is board certified in Pediatric Endocrinology.
David Ramirez is an Ophthalmologist practicing medicine in Chicago, Illinois. He has been practicing medicine for over 8 years. Dr. Ramirez is rated as an Experienced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Strabismus, Amblyopia, Papilledema, and Esotropia. Dr. Ramirez is board certified in American Board Of Ophthalmology - Ophthalmology (Certified).
517 Moye Medical Center-Adult And Pediatric Health Care
Lacy Hobgood is a primary care provider, practicing in Internal Medicine in Greenville, North Carolina. Dr. Hobgood is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Type 2 Diabetes (T2D), Familial Hypertension, Endoscopy, and Gastrostomy.
C. S. Mott Children's Hospital
Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ahmad is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. 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.
Domino's Farms
Tomoyasu Higashimoto is a Medical Genetics specialist and an Internal Medicine provider practicing medicine in Ann Arbor, Michigan. Dr. Higashimoto is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. He is also highly rated in 110 other conditions, according to our data. His clinical expertise encompasses Nevoid Basal Cell Carcinoma Syndrome, Methylmalonic Acidemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Propionic Acidemia. Dr. Higashimoto is board certified in Family Medicine and Clinical Genetics & Genomics.
Domino's Farms
Dr. Lee earned her M.D. from Ross University School of Medicine in 2013, and completed Pediatric Residency at Ascension St. John Hospital in Grosse Point, MI, where she served as a Chief Pediatric Resident during her final year of residency. She completed Categorical Medical Genetics Residency at the University of Michigan in 2019. Following this she accepted a dual faculty position as a Clinical Lecturer in the Department of Pediatrics and Department of Internal Medicine for one year, before returning to Fellowship in 2020 to complete additional dedicated training in Medical Biochemical Genetics. After completion of Medical Biochemical Genetics Fellowship, she resumed her faculty position as a Clinical Assistant Professor in 2021. She is board certified in Pediatrics, and in Clinical and General Genetics.She has a dual faculty appointment in the Department of Pediatrics and the Department of Internal Medicine. As a faculty member in the Department of Pediatrics, she sees patients in the Pediatric Genetics and Biochemical Genetics Clinics, in addition to the newly created Multidisciplinary Genetics of Hearing Loss Clinic. As a faculty member in the Department of Internal Medicine, she sees patients in the Adult Medical Genetics and Cancer Genetics Clinics, in addition to patients with atypical diabetes and/or lipodystrophy in collaboration with MEND.In addition to her clinical responsibilities, Dr. Lee also enjoys spending time teaching and discussing various aspects of genetics with fellows, pediatric residents, medical students, and genetic counseling students. Dr. Lee is rated as an Advanced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 138 other conditions, according to our data. Her clinical expertise encompasses Biotinidase Deficiency, Delayed Growth, Beta-Ketothiolase Deficiency, and Triple X Syndrome. Dr. Lee is board certified in Pediatrics, Clinical Genetics & Genomics, and Medical Biochemical Genetics.
Children's Mercy Kansas City
Nitin Madan is a Pediatric Cardiologist practicing medicine in Kansas City,, Missouri. Dr. Madan is rated as an Experienced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Congenital Coronary Artery Malformation, Anomalous Left Coronary Artery from the Pulmonary Artery, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.
UT Southwestern - Pediatric Genetics
Angela Scheuerle is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Dallas, Texas. Dr. Scheuerle is rated as an Experienced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 170 other conditions, according to our data. Her clinical expertise encompasses Hennekam Syndrome, Fetal Akinesia Sequence, Hemihyperplasia, and Incontinentia Pigmenti.
Ann & Robert H. Lurie Children's Hospital Of Chicago
Joyce Wu is a Neurologist practicing medicine in Chicago, Illinois. Dr. Wu is rated as an Experienced provider by MediFind in the treatment of Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. She is also highly rated in 12 other conditions, according to our data. Her clinical expertise encompasses Epilepsy in Children, Autism Spectrum Disorder, Orofaciodigital Syndrome 6, and Hydranencephaly.
Last Updated: 04/28/2026







