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.
Original language | English |
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Pages (from-to) | 347-351 |
Number of pages | 5 |
Journal | Journal of Inherited Metabolic Disease |
Volume | 29 |
Issue number | 2-3 |
DOIs | |
Publication status | Published - 2006 Apr 1 |
Externally published | Yes |
Subject classification (UKÄ)
- Neurology