The 20 Best Citrullinemia Doctors Near Me in Los Angeles, CA
Find the Top Citrullinemia Experts and Specialists
The 20 Best Citrullinemia Doctors near Los Angeles, CA
MediFind found 5 doctor with experience in Citrullinemia near Los Angeles, CA. Of these, 4 are Experienced and 1 are Advanced.
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 Citrullinemia. His top areas of expertise are Adrenoleukodystrophy (ALD), Classic Galactosemia, Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Vats is currently accepting new patients.
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 Citrullinemia. His top areas of expertise are Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Triple X Syndrome, and Chromosome 10q Deletion.
Stephen Cederbaum is a Medical Genetics provider in Los Angeles, California. Dr. Cederbaum is rated as an Experienced provider by MediFind in the treatment of Citrullinemia. His top areas of expertise are Arginase Deficiency, Urea Cycle Disorders (UCD), Phenylketonuria (PKU), and Argininosuccinic Aciduria.
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 Citrullinemia. His top areas of expertise are Multiple Sulfatase Deficiency, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Gaucher Disease, and Gaucher Disease Type 1. Dr. Longo is currently accepting new patients.
Uc Regents
Derek Wong is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Wong is rated as an Experienced provider by MediFind in the treatment of Citrullinemia. His top areas of expertise are Von Gierke Disease, Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Ornithine Transcarbamylase Deficiency.
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Last Updated: 02/22/2026