The 20 Best Glycine Encephalopathy Doctors Near Me in palo alto, CA
Find the Top Glycine Encephalopathy Experts and Specialists
Lpch Medical Group Div Of Lucile
Chung Lee is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. She has been practicing medicine for over 18 years. Dr. Lee is rated as an Advanced provider by MediFind in the treatment of Glycine Encephalopathy. She is also highly rated in 45 other conditions, according to our data. Her clinical expertise encompasses Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, Maple Syrup Urine Disease, and Carnitine Palmitoyltransferase 2 Deficiency.
Lpch Medical Group Div Of Lucile
Gregory Enns is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Enns is rated as an Experienced provider by MediFind in the treatment of Glycine Encephalopathy. He is also highly rated in 54 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Methylmalonic Acidemia, Arginase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Dr. Enns is currently accepting new patients.
Lpch Medical Group Div Of Lucile
Anne Niehaus is a Medical Genetics provider practicing medicine in Palo Alto, California. Dr. Niehaus is rated as an Experienced provider by MediFind in the treatment of Glycine Encephalopathy. She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Microcephaly, Cardiomyopathy Hypogonadism Metabolic Anomalies, WAGR Syndrome, and Atelosteogenesis Type 1.
Natalia Gomez-Ospina is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Gomez-Ospina is rated as an Experienced provider by MediFind in the treatment of Glycine Encephalopathy. She is also highly rated in 10 other conditions, according to our data. Her clinical expertise encompasses Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Incontinentia Pigmenti, Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), and Myhre Syndrome.
Last Updated: 09/26/2026