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Treatment with amino acids in serine deficiency disorders.

Authors :
de Koning TJ
Source :
Journal of inherited metabolic disease [J Inherit Metab Dis] 2006 Apr-Jun; Vol. 29 (2-3), pp. 347-51.
Publication Year :
2006

Abstract

Serine deficiency disorders are rare defects in the biosynthesis of the amino acid L-serine. At present two disorders have been reported: 3-phosphoglycerate dehydrogenase deficiency and 3-phosphoserine phosphatase deficiency. These enzyme defects lead to severe neurological symptoms such as congenital microcephaly and severe psychomotor retardation and in addition in patients with 3-phosphoglycerate dehydrogenase deficiency to intractable seizures. These symptoms respond to a variable degree to treatment with L-serine, sometimes combined with glycine. In this paper the current practice of amino acid treatment with L-serine and glycine in serine deficiency is reviewed.

Details

Language :
English
ISSN :
1573-2665
Volume :
29
Issue :
2-3
Database :
MEDLINE
Journal :
Journal of inherited metabolic disease
Publication Type :
Academic Journal
Accession number :
16763900
Full Text :
https://doi.org/10.1007/s10545-006-0269-0