The 20 Best Phenylketonuria (PKU) Doctors Near Me in Los Angeles, CA
Find the Top Phenylketonuria (PKU) Experts and Specialists
MediFind found 11 doctor with experience in Phenylketonuria (PKU) near Los Angeles, CA. Of these, 6 are Experienced, 3 are Advanced and 2 are Distinguished.
USC Care Medical Group Inc
Shoji Yano is a Medical Genetics provider in Los Angeles, California. Dr. Yano is rated as a Distinguished provider by MediFind in the treatment of Phenylketonuria (PKU). His top areas of expertise are Phenylketonuria (PKU), Infantile Refsum Disease, Methylmalonic Acidemia, and Maternal Hyperphenylalaninemia.
Kaiser Permanente Los Angeles Medical Center - Genetics Department
Divya Vats is a Medical Genetics provider in Los Angeles, California. Dr. Vats is rated as an Advanced provider by MediFind in the treatment of Phenylketonuria (PKU). His top areas of expertise are Adrenoleukodystrophy (ALD), Classic Galactosemia, Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Vats is currently accepting new patients.
Office
Rukmani Vasan is a Pediatrics provider in Los Angeles, California. Dr. Vasan is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). Her top area of expertise is Phenylketonuria (PKU).
Linda Randolph is a Medical Genetics provider in Los Angeles, California. Dr. Randolph is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). Her top areas of expertise are Neurofibromatosis, Chromosome 11 Uniparental Disomy, Chromosome 6q Duplication, and Chromosome 8p Deletion.
Southern California Permanente Medical Group
Moin Vera is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Vera is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). His top areas of expertise are Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Triple X Syndrome, and Chromosome 10q Deletion.
Rebecca Mardach is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Mardach is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). Her top areas of expertise are Gaucher Disease Type 1, Gaucher Disease, Propionic Acidemia, and Farber Lipogranulomatosis.
Stephen Cederbaum is a Medical Genetics provider in Los Angeles, California. Dr. Cederbaum is rated as a Distinguished provider by MediFind in the treatment of Phenylketonuria (PKU). His top areas of expertise are Urea Cycle Disorders (UCD), Arginase Deficiency, Phenylketonuria (PKU), and Argininosuccinic Aciduria.
Uc Regents
Derek Wong is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Wong is rated as an Advanced provider by MediFind in the treatment of Phenylketonuria (PKU). His top areas of expertise are Von Gierke Disease, Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Ornithine Translocase Deficiency.
Cedars-Sinai Primary Care-Marina Del Rey
William Lang is a primary care provider, practicing in Internal Medicine in Marina Del Rey, California. Dr. Lang is rated as an Advanced provider by MediFind in the treatment of Phenylketonuria (PKU). His top areas of expertise are Phenylketonuria (PKU), Hereditary Ataxia, Osteomyelitis in Children, and West Nile Virus Infection.
Uc Regents
Nicola Longo is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Longo is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). His top areas of expertise are Multiple Sulfatase Deficiency, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Gaucher Disease Type 3, and Gaucher Disease Type 1. Dr. Longo is currently accepting new patients.
Uc Regents
Bianca Russell is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Russell is rated as an Experienced provider by MediFind in the treatment of Phenylketonuria (PKU). Her top areas of expertise are Chromosome 4p Deletion, Wolf-Hirschhorn Syndrome, Congenital Athymia, and Toriello-Carey Syndrome.
Last Updated: 04/28/2026