期刊
IUBMB LIFE
卷 61, 期 1, 页码 27-34出版社
WILEY
DOI: 10.1002/iub.137
关键词
G6PD assay; favism; molecular test; diagnosis; pyruvate kinase; G6PD/6PGD
Glucose 6-phosphate dehydrogenase (G6PD) deficiency is the most common defect of red blood cells. Although some different laboratory techniques or methods are employed for the biochemical screening, a strict relationship between biochemists, clinicians, and molecular biologists is necessary for a definitive diagnosis. This article represents an overview on the current laboratory tests finalized to the screening or to the definitive diagnosis of G6PD-deficiency, underlying the problems regarding the biochemical and molecular identification of heterozygote females other than those regarding the standardization of the clinical and laboratory diagnostic procedures. Finally, this review is aimed to give a flow-chart for the complete diagnostic approach or G6PD-deficiency. (C) 2008 IUBMB
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