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范可尼贫血:南非阿非利卡人群中另一种患病率异常高的疾病。

Fanconi anemia: another disease of unusually high prevalence in the Afrikaans population of South Africa.

作者信息

Rosendorff J, Bernstein R, Macdougall L, Jenkins T

机构信息

Department of Human Genetics, School of Pathology, South African Institute for Medical Research, Johannesburg.

出版信息

Am J Med Genet. 1987 Aug;27(4):793-7. doi: 10.1002/ajmg.1320270408.

Abstract

We have investigated the prevalence of homozygous and heterozygous Fanconi anemia (FA) in the Afrikaans community of the southern Transvaal Province. The minimum birth incidence of FA in white, Afrikaans-speaking South Africans was estimated to be 1 in 22,000, with the calculated heterozygote prevalence being approximately 1 in 77. Alternatively, based on a point prevalence of 1 in 26,000, the carrier rate may be estimated as 1 in 83. It is postulated that this unusually high frequency of the gene for FA is attributable to founder effect.

摘要

我们调查了德兰士瓦省南部南非荷兰语社区中纯合子和杂合子范可尼贫血(FA)的患病率。估计讲南非荷兰语的白人中FA的最低出生发病率为22000分之一,计算得出的杂合子患病率约为77分之一。或者,根据26000分之一的现患率,携带者率可估计为83分之一。据推测,FA基因这种异常高的频率归因于奠基者效应。

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