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(East. Mediterr. health j).
em Inglês | WHO IRIS | ID: who-119135

RESUMO

We attempted to characterize biochemically glucose-6-phosphate dehydrogenase [G6PD] variants in Iraqi individuals. Thus 758 healthy Iraqi males aged 18-60 years were randomly selected and 46 [6.1%] were G6PD deficient. Although the predominant non-deficient G6PD phenotype was G6PD B [92.6%], G6PD A+ was found in polymorphic frequency [1.3%]. In the deficient group, 31 cases were fully characterized, including 17 cases with features consistent with G6PD Mediterranean variant, while 12 had other biochemical features and were labelled as non-Mediterranean variant. The remaining two deficient cases were characterized as G6PD A- variant. The presence of a significant number of non-Mediterranean variant was unexpected and may be related to the more heterogeneous background of the Iraqi people


Assuntos
Estudos de Casos e Controles , Eletroforese em Acetato de Celulose , Epidemiologia Molecular , Eritrócitos , Favismo , Frequência do Gene , Glucosefosfato Desidrogenase , Fenótipo , Polimorfismo Genético , Deficiência de Glucosefosfato Desidrogenase
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