Ciofu E, Mironeanu T
Institute of Hygiene and Medical Research, Iaşi, Romania.
Rev Med Chir Soc Med Nat Iasi. 1992 Jul-Dec;96(3-4):215-7.
Between 1985 and 1989, a sample of 13,710 subjects (5,825 males and 7,885 females) from the Vrancea, Bacău, Neamţ and Suceava districts were examined for the presence of this pathological gene, 32 male hemizygotes and 13 female heterozygotes and homozygotes being detected. The incidence of G-6-PD deficit in the hemizygotes was of 0.55%. The investigations carried out in the shifting gene carriers' families revealed the way deficit is transmitted to offsprings. Hemizygotes get it from their mother while the female homozygotes either from their mother or father. The frequency of G-6-PD deficit of 0.55% in a population sample of 13,710 subjects is within the limits established by Marcu and Schneer for our country (0.1-1.8%). By comparing the frequency of 0.55% in the Vrancea, Bacău, Neamţ and Suceava districts which formerly had an increased incidence of malaria (Galaţi - 4.01% and Huşi - 5.94%) its low value could be explained by the absence of malaria factor.
1985年至1989年间,对来自弗朗恰、巴克乌、尼亚姆茨和苏恰瓦地区的13710名受试者(5825名男性和7885名女性)进行了检查,以确定是否存在这种致病基因,共检测出32名男性半合子以及13名女性杂合子和纯合子。半合子中G-6-PD缺乏症的发病率为0.55%。对携带转移基因的家庭进行的调查揭示了该缺乏症向后代的传递方式。半合子从母亲那里遗传该病症,而女性纯合子则要么从母亲要么从父亲那里遗传。在13710名受试者的群体样本中,G-6-PD缺乏症的频率为0.55%,处于马尔库和施内尔为我国确定的范围(0.1 - 1.8%)之内。通过比较弗朗恰、巴克乌、尼亚姆茨和苏恰瓦地区(这些地区以前疟疾发病率较高,加拉茨为4.01%,胡希为5.94%)0.55%的频率,其低值可归因于疟疾因素的不存在。