MediFind found 5 doctor with experience in 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency near Massachusetts, US. Of these, 4 are Experienced and 1 are Advanced.
Children's Hospital Pediatric Associates, Inc
Stephanie Sacharow is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Sacharow 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 Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Cat Eye Syndrome, and Dihydropteridine Reductase Deficiency. Dr. Sacharow is currently accepting new patients.
Children's Hospital Pediatric Associates, Inc
Melinda Peters is a Medical Genetics provider in Boston, Massachusetts. Dr. Peters 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 N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3, Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome).
Children's Hospital Pediatric Associates, Inc
Olaf Bodamer is a Medical Genetics provider in Boston, Massachusetts. Dr. Bodamer 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 Kabuki Syndrome, Classic Galactosemia, Niemann-Pick Disease, and Mucopolysaccharidoses (MPS). Dr. Bodamer is currently accepting new patients.
Anne O'donnell-Luria is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. O'donnell-Luria 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 Chromosome 11 Uniparental Disomy, Mosaic Variegated Aneuploidy Syndrome, Chromosome 2 Uniparental Disomy, and Tetrasomy 9p. Dr. O'donnell-Luria is currently accepting new patients.
Massachusetts General Physicians Organization Inc
David Sweetser is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Sweetser 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 Hypotonia, Ornithine Transcarbamylase Deficiency, Ornithine Translocase Deficiency, and Propionic Acidemia. Dr. Sweetser is currently accepting new patients.
Last Updated: 10/30/2025