The 20 Best 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency Doctors Near Me
Find the Top 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency Experts and Specialists
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 8 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 1 Deficiency, Carnitine Palmitoyltransferase 2 Deficiency, and Urea Cycle Disorders (UCD).
Duke Health Integrated Practice Inc
Dmitriy Niyazov is a Medical Genetics provider practicing medicine in Durham, North Carolina. Dr. Niyazov is rated as an Experienced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. He is also highly rated in 9 other conditions, according to our data. His clinical expertise encompasses Early Infantile Epileptic Encephalopathy, Thymidine Kinase 2 Deficiency (TK2d), Macroglossia, and Ehlers-Danlos Syndrome (EDS). Dr. Niyazov is board certified in American Board Of Medical Genetics And Genomics, Clinical Genetics And Genomics - General. Dr. Niyazov is currently accepting new patients.
Carolina Fernandes practices practicing medicine in Sao Paulo, 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, Glutaric Acidemia Type 1, Vaginal Yeast Infection, and Vulvovaginitis.
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 Glycogen Storage Disease Type 6, Mitochondrial Trifunctional Protein Deficiency, Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
Tanyel Zubarioglu practices practicing medicine in Istanbul, Turkey. Ms. Zubarioglu 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 13 other conditions, according to our data. Her clinical expertise encompasses Xanthoma, Cerebrotendinous Xanthomatosis, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Maple Syrup Urine Disease.
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 Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Urea Cycle Disorders (UCD), and Ornithine Transcarbamylase 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, Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Carnitine Palmitoyltransferase 1 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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Carnitine Palmitoyltransferase 1 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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Carnitine Palmitoyltransferase 1 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.
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).
Kagan Calisgan practices practicing medicine in Cerrahpasa, Turkey. Mr. Calisgan 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 3 other conditions, according to our data. His clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Cerebrotendinous Xanthomatosis, Xanthoma, and Primary Carnitine Deficiency.
M Health Fairview Explorer Pediatric Specialty Clinic
Susan Berry is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Minneapolis, Minnesota. Dr. Berry 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 19 other conditions, according to our data. Her clinical expertise encompasses Propionic Acidemia, Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Alkaptonuria. 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.
C. S. Mott Children's Hospital
Jesse Thoene is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Thoene 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 2 other conditions, according to our data. His clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Argininosuccinic Aciduria, Glycine Encephalopathy, and Inborn Amino Acid Metabolism Disorder. Dr. Thoene is board certified in Pediatrics and Clinical Biochemical Genetics. Dr. Thoene is currently accepting new patients.
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 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. She is also highly rated in 45 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Danon Disease, Von Gierke Disease, and Tyrosinemia Type 3. Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics. Dr. Ahmad is currently accepting new patients.
Sanford Fetal Care Center Sioux Falls
Laura Davis-Keppen is a Pediatric Endocrinologist and a Medical Genetics provider practicing medicine in Sioux Falls, South Dakota. Dr. Davis-Keppen 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), 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Argininosuccinic Aciduria, and Dihydropteridine Reductase Deficiency. Dr. Davis-Keppen is board certified in American Board Of Medical Genetics: Clinical GeneticsAmerican Board Of Pediatrics: Pediatric EndocrinologyAmerican Board Of Pediatrics: Pediatrics. Dr. Davis-Keppen is currently accepting new patients.
Emory Clinic At 1365 Clifton Road
William Wilcox is a Medical Genetics provider practicing medicine in Atlanta, Georgia. 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 25 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. Dr. Wilcox is currently accepting new patients.
Last Updated: 09/26/2026