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3-phosphoglycerate dehydrogenase deficiency in a patient with West syndrome

Published online by Cambridge University Press:  03 October 2000

M Pineda
Affiliation:
S. Neuropediatria i Bioquímica, Unitat Integrada, Hospital Sant Joan de Déu/Hospital Clínic, Universitat de Barcelona , Barcelona, Spain.
M A Vilaseca
Affiliation:
S. Neuropediatria i Bioquímica, Unitat Integrada, Hospital Sant Joan de Déu/Hospital Clínic, Universitat de Barcelona , Barcelona, Spain.
R Artuch
Affiliation:
S. Neuropediatria i Bioquímica, Unitat Integrada, Hospital Sant Joan de Déu/Hospital Clínic, Universitat de Barcelona , Barcelona, Spain.
S Santos
Affiliation:
S. Neuropediatria i Bioquímica, Unitat Integrada, Hospital Sant Joan de Déu/Hospital Clínic, Universitat de Barcelona , Barcelona, Spain.
M M García González
Affiliation:
Cap de Banyolas i Hospital de Figueres, Barcelona, Spain.
I Sau
Affiliation:
Cap de Banyolas i Hospital de Figueres, Barcelona, Spain.
A Aracil
Affiliation:
S. Neuropediatria i Bioquímica, Unitat Integrada, Hospital Sant Joan de Déu/Hospital Clínic, Universitat de Barcelona , Barcelona, Spain.
E Van Schaftingen
Affiliation:
Institute of Cellular and Molecular Pathology, Brussels, Belgium.
J Jaeken
Affiliation:
Department of Paediatrics, Center for Metabolic Disease, University Hospital Gasthuisberg, Leuven, Belgium.
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Abstract

3-phosphoglycerate dehydrogenase deficiency is a severe but treatable disorder of serine synthesis, first described in 1996 (Jaeken et al. 1996a). The patient presented with West syndrome, severe psychomotor delay, failure to thrive, microcephaly, atypical ocular movements, and pyramidal signs. Treatment with oral L-serine abolished seizures and improved psychomotor development, hyperexcitability, head growth, cortical and subcortical hypotrophy, and hypomyelination of the brain on MRI scans. 3-phosphoglyce-rate dehydrogenase deficiency is a treatable congential error that probably leads to West syndrome.

Type
Case Reports
Copyright
© 2000 Mac Keith Press

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