Erythrocyte Glucose‐6‐Phosphate Dehydrogenase Deficiency in Turkey
Erythrocyte Glucose‐6‐Phosphate Dehydrogenase Deficiency in Turkey
复制标题
火鸡红细胞葡萄糖-6-磷酸脱氢酶缺乏症
DOI：
10.1111/j.1651-2227.1965.tb06378.x
复制
发表时间：
1965
期刊：
影响因子：
--
通讯作者：
N. Çevik
中科院分区：
文献类型：
--
作者：
B. Say;P. Ozand;Í. Berkel;N. Çevik
在一次前瞻性的交流中，我们报道了土耳其第一个报道的新生儿黄疸病例，即一名男婴的G-6-PD缺乏症[16]。这种酶缺陷的发生率在不同的种族群体中似乎有很大差异。然而，众所周知，这种缺陷在地中海人中的患病率要高得多，特别是在希腊人、犹太人、西西里人、撒丁岛人和阿拉伯人中。据我们所知，沙特阿拉伯的发病率最高(65.4 7，；)[XI.据报道，非洲和美国黑人、亚裔印度人和中国人也有相当高的发病率。
In a, prcvious communication, we pr+ sented the first roported case of neonatal jaundice t h e to G-6-PD deficiency in a newborn male infant in Turkey [16]. T h e incidence of this cnzymatic defect seems to vary markedly in different racial groups. However, i t is well established that the prevalence of this defect is significantly higher in t’he Mediterranean people, particularly among the Greeks, Jews, Sicilians, Sardinians, and Arabs. To the best of our knowledge, the highest rate of incidence (65.4 7,;) u-as reported from Saudi Arabia [X I . African and American negroes, Asiatic Indians and Chinese are also reported to have a rather high incidence of this defect