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PubMed · 17222195

PGK deficiency.

Ernest Beutler
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Abstract

Phosphoglycerate kinase (PGK) deficiency is one of the relatively uncommon causes of hereditary non-spherocytic haemolytic anaemia (HNSHA). The gene encoding the erythrocyte enzyme PGK1, is X-linked. Mutations of this gene may cause chronic haemolysis with or without mental retardation and they may cause myopathies, often with episodes of myoglobinuria, or a combination of these clinical manifestations. Twenty-six families have been described and in 20 of these the mutations are known. The reason for different clinical manifestations of mutations of the same gene remains unknown.

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Anemia, Hemolytic, Congenital NonspherocyticBase SequenceGenetic Diseases, X-LinkedHumansMolecular Sequence DataMutationPhosphoglycerate KinaseProtein ConformationJournal ArticleResearch Support, Non-U.S. Gov'tReview

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BibTeXRIS

Ernest Beutler. 2007. PGK deficiency.. https://doi.org/10.1111/j.1365-2141.2006.06351.x

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