| Literature DB >> 9708551 |
T J de Koning1, M Duran, L Dorland, R Gooskens, E Van Schaftingen, J Jaeken, N Blau, R Berger, B T Poll-The.
Abstract
3-Phosphoglycerate dehydrogenase (3-PGDH) deficiency is an inborn error of serine biosynthesis. Patients are affected with congenital microcephaly, psychomotor retardation, and intractable seizures. The effects of oral treatment with amino acids were investigated in 2 siblings. L-Serine up to 500 mg/kg/day was not sufficient for seizure control. Addition of glycine 200 mg/kg/day resulted in complete disappearance of seizures. Electroencephalographic abnormalities gradually resolved after 6 months. We conclude that 3-PGDH can be treated effectively by a combination of L-serine and glycine.Entities:
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Year: 1998 PMID: 9708551 DOI: 10.1002/ana.410440219
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422