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Can African-variant G6PD deficiency trigger hemolysis in DKA?

✍ Scribed by Ranjit K. Goudar; Scott J. Samuelson; Arashk Motiei; Srobona T. Chatterjee

Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
137 KB
Volume
78
Category
Article
ISSN
0361-8609

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G-6PD β€œankara”. A new G-6PD variant with
G-6PD β€œankara”. A new G-6PD variant with deficiency found in a Turkish family
✍ Axel Kahn; M. L. North; J. Messer; P. Boivin πŸ“‚ Article πŸ“… 1975 πŸ› Springer 🌐 English βš– 317 KB

A new G-6PD varient with enzyme deficiency is described in a 7-month-old Turkish boy without any hemolytic manifestation, except neonatal hyperbilirubinemia. The main characteristics of this variant were the following: Severe enzyme deficiency in erythrocytes (8% of normal), fast starch-gel-electrop