The 20 Best Carnitine Palmitoyltransferase 2 Deficiency Doctors Near Me in Los Angeles, CA
Find the Top Carnitine Palmitoyltransferase 2 Deficiency Experts and Specialists
Transplant Services-Heart At Los Angeles Medical Center
Ronald Rosengart is a Pediatric Cardiologist practicing medicine in Los Angeles, California. Dr. Rosengart is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Ventricular Septal Defects, Heart Murmurs, Tetralogy of Fallot, and Myocarditis.
Kaiser Permanente Los Angeles Medical Center - Genetics Department
Divya Vats is a Medical Genetics provider practicing medicine in Los Angeles, California. Dr. Vats is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. He is also highly rated in 24 other conditions, according to our data. His clinical expertise encompasses Adrenoleukodystrophy (ALD), Classic Galactosemia, Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Vats is currently accepting new patients.
Southern California Permanente Medical Group
Moin Vera is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Los Angeles, California. Dr. Vera is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Triple X Syndrome, and Chromosome 10q Deletion.
Uc Regents
Derek Wong is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Los Angeles, California. Dr. Wong is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 2 Deficiency. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Von Gierke Disease, Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Ornithine Translocase Deficiency.
Last Updated: 04/28/2026