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Inherited anaemias in the Greek community of Cape Town.

机译:在开普敦希腊社区遗传性贫血。

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摘要

Cape Town has a Greek community of about 5000, of whom approximately 75% originate from the island of Lesbos. In a survey of inherited haematological conditions in this population, 250 unrelated volunteers were investigated. The prevalence of heterozygous beta-thalassaemia was found to be 6.4%, with a gene frequency of 0.033. G6PD deficiency was detected in 10 males and it can be estimated that the prevalence in the male members of this population is 6.7%, with a gene frequency of 0.067. Hereditary spherocytosis was found in three respondents and this represents a prevalence of 1.2%, with a gene frequency of 0.006. One subject was heterozygous for the sickle cell trait (HbS) and another volunteer had haemoglobin Lepore, which had already been diagnosed in Greece. Our findings with respect to beta-thalassaemia and G6PD deficiency are similar to those reported from regions in Greece where malaria is not highly endemic.
机译:开普敦拥有约5000个希腊社区,其中约75%来自莱斯博斯岛。在对该人群的遗传性血液学状况进行的一项调查中,对250名无关的志愿者进行了调查。发现杂合性β-地中海贫血的患病率为6.4%,基因频率为0.033。在10名男性中检测到G6PD缺乏症,据估计该人群中男性成员的患病率为6.7%,基因频率为0.067。在三个受访者中发现了遗传性球囊菌病,这表示患病率为1.2%,基因频率为0.006。一名受试者的镰状细胞性状(HbS)为杂合子,另一名受试者的血红蛋白Lepore已在希腊被确诊。我们关于β地中海贫血和G6PD缺乏症的发现与希腊疟疾不是高度流行的地区的报道相似。

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