色雷斯西部土耳其人群血红蛋白变异体、β地中海贫血、葡萄糖-6-磷酸脱氢酶缺乏症及触珠蛋白类型的调查
Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace.
作者信息
Aksoy M, Kutlar A, Kutlar F, Dinçol G, Erdem S, Baştesbihçi S
出版信息
J Med Genet. 1985 Aug;22(4):288-90. doi: 10.1136/jmg.22.4.288.
Abstract
A total of 102 apparently healthy and randomly selected Turks who either immigrated from Western Thrace or were still living there were studied for haemoglobin variants, high Hb A2 beta thalassaemia, G6PD deficiency, and haptoglobin types. The incidence of haemoglobins S and O Arab were 2.9 and 3.9% respectively. The incidence of high A2 beta thalassaemia was 10.8% and that of G6PD deficiency 5%. The gene frequencies of Hp1 and Hp2 were 0.326 and 0.674, respectively.
摘要
对102名明显健康且随机选取的土耳其人进行了研究，这些人要么是从西色雷斯移民而来，要么仍居住在那里，研究内容包括血红蛋白变体、高Hb A2β地中海贫血、葡萄糖-6-磷酸脱氢酶（G6PD）缺乏症以及触珠蛋白类型。血红蛋白S和阿拉伯型血红蛋白O的发生率分别为2.9%和3.9%。高A2β地中海贫血的发生率为10.8%，G6PD缺乏症的发生率为5%。触珠蛋白1（Hp1）和触珠蛋白2（Hp2）的基因频率分别为0.326和0.674。
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