The 20 Best 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency Doctors Near Me in Boston, MA
Find the Top 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency Experts and Specialists
Massachusetts General Physicians Organization Inc
David Sweetser is a Pediatrics provider practicing medicine in Boston, Massachusetts. Dr. Sweetser 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 10 other conditions, according to our data. His clinical expertise encompasses Hypotonia, Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, and Propionic Acidemia. Dr. Sweetser is board certified in Pediatrics, Clinical Biochemical Genetics, Pediatric Hematology-Oncology, and Clinical Genetics And Genomics.
Children's Hospital Pediatric Associates, Inc
Melinda Peters is a Medical Genetics provider practicing medicine in Boston, Massachusetts. Dr. Peters is rated as an Experienced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. She is also highly rated in 32 other conditions, according to our data. Her clinical expertise encompasses N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3, Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), and Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome).
Children's Hospital Pediatric Associates, Inc
Olaf Bodamer is a Medical Genetics provider practicing medicine in Boston, Massachusetts. Dr. Bodamer 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 51 other conditions, according to our data. His clinical expertise encompasses Kabuki Syndrome, Classic Galactosemia, Niemann-Pick Disease, and Microcephaly. Dr. Bodamer is currently accepting new patients.
Anne O'donnell-Luria is a Medical Genetics specialist and a Pediatrics provider practicing medicine 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. She is also highly rated in 8 other conditions, according to our data. Her clinical expertise encompasses Chromosome 11 Uniparental Disomy, Pallister-Killian Mosaic Syndrome, Chromosome 6 Uniparental Disomy, and Chromosome 2 Uniparental Disomy. Dr. O'donnell-Luria is currently accepting new patients.
Last Updated: 04/28/2026