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Failure of Leucovorin therapy in nonketotic hyperglycinemia

✍ Scribed by Stephen P. Spielberg; Anne W. Lucky; Joseph D. Schulmar; Lloyd I. Kramer; Lawrence Hefter; Stephen I. Goodman

Book ID
118539140
Publisher
Elsevier Science
Year
1976
Tongue
English
Weight
190 KB
Volume
89
Category
Article
ISSN
1097-6833

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Nonketotic hyperglycinemia (NKH) is an inborn error of metabolism characterized by accumulation of glycine in body fluids and various neurological symptoms. NKH is caused by deficiency of the glycine cleavage multi-enzyme system with three specific components encoded by GLDC, AMT, and GCSH. We under