GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY AND THE SICKLE-CELL GENE IN MAKKAH, SAUDI-ARABIA

被引:13
|
作者
ELHAZMI, MAF
WARSY, AS
BAHAKIM, HH
ALSWAILEM, A
机构
[1] COLL MED, WHO, COLLABORATING CTR, RIYADH, SAUDI ARABIA
[2] KING SAUD UNIV, COLL SCI, DEPT BIOCHEM, RIYADH, SAUDI ARABIA
[3] MINIST HLTH, RIYADH, SAUDI ARABIA
[4] COLL MED, DEPT PAEDIAT, RIYADH, SAUDI ARABIA
[5] KING SAUD UNIV, KING KHALID UNIV HOSP, RIYADH, SAUDI ARABIA
关键词
D O I
10.1093/tropej/40.1.12
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
This study was conducted on 689 Saudi males and females living in the Makkah area in the western province of Saudi Arabia. The frequency of severe glucose-6-phosphate dehydrogenase (G-6-PD) deficiency in the male and female populations was 0.055 and 0.042 respectively. The normal G-6-PD was G-6-PD-B+ and the G-6-PD phenotypes identified included G-B-PD-A(+), G-6-PD-A(-), G-6-PD-Mediterranean, and G-6-PD-Mediterranean-like at gene frequencies of 0.0288, 0.0026, 0.05497, and 0.1969 in the male population and 0.026, 0.0146, 0.0407, and 0.02606 in the female population. The main variants producing severe and mild G-6-PD deficiency were G-6-PD-Mediterranean and G-6-PD-Mediterranean-like, respectively. The sickle cell gene was identified at a frequency of 0.029 and no interaction between sickle cell and G-6-PD deficiency genes was encountered.
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页码:12 / 16
页数:5
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