The 20 Best 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency Doctors Near Me

Grant Mitchell practices practicing medicine in Montreal, Canada. Mr. Mitchell is rated as an Elite expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Mckusick-Kaufman Syndrome, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Transcobalamin Deficiency, Polymicrogyria, and Liver Transplant.

Moacir Wajner practices practicing medicine in Porto Alegre, Brazil. Wajner is rated as an Elite expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. They are also highly rated in 25 other conditions, according to our data. Their clinical expertise encompasses Medium-Chain Acyl-CoA Dehydrogenase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Glutaric Acidemia Type 1, and Sulfite Oxidase Deficiency.

Jan Vaclavik practices practicing medicine in Ostrava, Czech Republic. Vaclavik is rated as an Elite expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. They are also highly rated in 4 other conditions, according to our data. Their clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Hypertension, Hyperaldosteronism, Kidney Transplant, and Cardiac Ablation.

Dominique Roland practices practicing medicine in Gosselies, Belgium. Roland is rated as an Elite expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. They are also highly rated in 1 other condition, according to our data. Their clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Carnitine Palmitoyltransferase 2 Deficiency, Carnitine Palmitoyltransferase 1 Deficiency, and Urea Cycle Disorders (UCD).

William Wilcox is a Medical Genetics provider practicing medicine in Atlanta, Georgia. He has been practicing medicine for over 38 years. Dr. Wilcox is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 26 other conditions, according to our data. His clinical expertise encompasses Fabry Disease, Achondroplasia, Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome). Dr. Wilcox is board certified in American Board Of Medical Genetics And Genomics, 1996.

Meral Gunay-Aygun is a professor of pediatrics and genetic medicine at Johns Hopkins University School of Medicine. Dr. Gunay-Aygun specializes in the diagnosis and treatment of children and adults with inherited metabolic diseases including diagnostic evaluation and follow-up of newborns with abnormal newborn screens for inherited metabolic diseases. After serving 14 years as an attending physician at The Johns Hopkins Hospital in Baltimore, she joined the medical staff of Johns Hopkins All Children’s Hospital in St. Petersburg, Florida in 2022. Dr. Gunay-Aygun earned her medical degree from Hacettepe University School of Medicine, Ankara, Turkey. She completed pediatrics and medical genetics residencies at Case Western Reserve University, Cleveland, Ohio, and a biochemical genetics fellowship at the National Institutes of Health’s National Human Genome Research Institute, Bethesda, Maryland. She has made numerous research contributions, especially in the study of inherited ciliopathies, for which she has earned international recognition. Dr. Gunay-Aygun received the Innovative Leadership Award from Genetic Alliance, as well as the NHGRI Merit Award for her research on Autosomal Recessive Polycystic Kidney Disease/Congenital Hepatic Fibrosis. She is a member of myriad professional organizations, including the American Society of Human Genetics, the American Academy of Pediatrics, the Society of Pediatric Research and the Society for Inherited Metabolic Disorders. Dr. Gunay is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Ornithine Transcarbamylase Deficiency, Ornithine Translocase Deficiency, and Argininosuccinic Aciduria. Dr. Gunay is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Carolina Fernandes practices practicing medicine in Porto Alegre, Brazil. Ms. Fernandes is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency and Glutaric Acidemia Type 1.

George Diaz is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Diaz is rated as a Distinguished provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 24 other conditions, according to our data. His clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Argininosuccinic Aciduria, Urea Cycle Disorders (UCD), and Ornithine Transcarbamylase Deficiency.

Sarah Grunert practices practicing medicine in Freiburg, Germany. Ms. Grunert is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. She is also highly rated in 33 other conditions, according to our data. Her clinical expertise encompasses Mitochondrial Trifunctional Protein Deficiency, Glycogen Storage Disease Type 6, Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.

Julie De Sousa practices practicing medicine in Olomouc, Czech Republic. Ms. De Sousa is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Carnitine Palmitoyltransferase 1 Deficiency, Medium-Chain Acyl-CoA Dehydrogenase Deficiency, and Adenylosuccinate Lyase Deficiency.

Tomas Adam practices practicing medicine in Olomouc, Czech Republic. Mr. Adam is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Carnitine Palmitoyltransferase 1 Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Adenylosuccinate Lyase Deficiency, and Medium-Chain Acyl-CoA Dehydrogenase Deficiency.

David Friedecky practices practicing medicine in Olomouc, Czech Republic. Mr. Friedecky is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Carnitine Palmitoyltransferase 1 Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Adenylosuccinate Lyase Deficiency, and Medium-Chain Acyl-CoA Dehydrogenase Deficiency.

Leo Kluijtmans practices practicing medicine in Nijmegen, Netherlands. Mr. Kluijtmans is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Cerebrotendinous Xanthomatosis, Xanthoma, and Orotic Aciduria Type 1.

Carmen Vargas practices practicing medicine in Porto Alegre, Brazil. Ms. Vargas is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses Maple Syrup Urine Disease, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Glutaric Acidemia Type 1, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).

Hao Yang practices practicing medicine in Zhongshan, China. Mr. Yang is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 31 other conditions, according to our data. His clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Liver Cancer, Lung Cancer, Laminectomy, and Hepato-Pancreato-Biliary Surgery.

Felix Bischof practices practicing medicine in Boeblingen, Germany. Mr. Bischof is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, CACH Syndrome, Progressive Multifocal Leukoencephalopathy, and Multiple Sclerosis (MS).

Maaike De Vries practices practicing medicine in Nijmegen, Netherlands. Ms. De Vries is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. She is also highly rated in 12 other conditions, according to our data. Her clinical expertise encompasses Galactokinase Deficiency, Classic Galactosemia, Galactose Epimerase Deficiency, and Galactosemia.

Jorn Sass practices practicing medicine in Rheinbach, Germany. Mr. Sass is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Beta-Ketothiolase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Canavan Disease.

Ron Wevers practices practicing medicine in Nijmegen, Netherlands. Mr. Wevers is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 23 other conditions, according to our data. His clinical expertise encompasses Xanthoma, Cerebrotendinous Xanthomatosis, Cutis Laxa, and Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency.

Daniella De Moura Coelho practices practicing medicine in Porto Alegre, Brazil. Ms. De Moura Coelho is rated as a Distinguished expert by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Maple Syrup Urine Disease, Orotic Aciduria Type 1, and Glutaric Acidemia Type 1.