G6PD MEDITERRANEAN ACCOUNTS FOR THE HIGH PREVALENCE OF G6PD DEFICIENCY IN KURDISH JEWS

Citation
A. Oppenheim et al., G6PD MEDITERRANEAN ACCOUNTS FOR THE HIGH PREVALENCE OF G6PD DEFICIENCY IN KURDISH JEWS, Human genetics, 91(3), 1993, pp. 293-294
Citations number
10
Categorie Soggetti
Genetics & Heredity
Journal title
ISSN journal
03406717
Volume
91
Issue
3
Year of publication
1993
Pages
293 - 294
Database
ISI
SICI code
0340-6717(1993)91:3<293:GMAFTH>2.0.ZU;2-O
Abstract
The Jews of Kurdistan are a small inbred population with a high incide nce of beta-thalassaemia and glucose-6-phosphate dehydrogenase (G6PD) deficiency. Recently, it was reported that the beta-thalassaemia in th is population shows an unusual mutational diversity; 13 different muta tions were identified, of which 4 had not previously been observed in any other population. In contrast, we now report that the G6PD deficie ncy, which has the highest known incidence in the world, and which aff ects about 70% of males, is almost entirely attributable to a single w idespread mutation, G6PD Mediterranean.