MediFind found 6 doctor with experience in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency near New York, US. Of these, 3 are Experienced, 2 are Advanced and 1 are Distinguished.
George Diaz is a Medical Genetics specialist and a Pediatrics provider 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. His top areas of expertise are 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Argininosuccinic Aciduria, Urea Cycle Disorders (UCD), and Ornithine Transcarbamylase Deficiency.
Icahn School Of Medicine At Mount Sinai
Margo Breilyn is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Breilyn is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Short-Chain Acyl-CoA Dehydrogenase Deficiency, and Tyrosinemia Type 1.
Icahn School Of Medicine At Mount Sinai
Ibrahim Elsharkawi is a Pediatrics specialist and a Medical Genetics provider in New York, New York. Dr. Elsharkawi is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are MELAS Syndrome, Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Tyrosinemia Type 2.
Icahn School Of Medicine At Mount Sinai
Jaya Ganesh is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Ganesh is rated as an Experienced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Pompe Disease, and Fabry Disease.
Icahn School Of Medicine At Mount Sinai
Mary Lopiccolo is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Lopiccolo is rated as an Experienced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Glutaric Acidemia Type 2, Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Carnitine Palmitoyltransferase 1 Deficiency.
Kimihiko Oishi is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Oishi is rated as an Experienced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Micrognathia, Citrullinemia, Urea Cycle Disorders (UCD), and Methylmalonic Acidemia with Homocystinuria.
Last Updated: 10/30/2025