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[匈牙利西部沃什州两种半乳糖血症类型的基因频率(作者译)]

[Gene frequencies of both forms of galactosaemia in the western Hungarian province of Vas (author's transl)].

作者信息

Sitzmann F C, Istvan L, Teubl I, Kaloud H, Cholnoky P

出版信息

Wien Klin Wochenschr. 1978 Jan 6;90(1):16-20.

PMID:204112
Abstract

The two enzymes of galactose metabolism, namely galactokinase and galactose-1-phosphate uridyltransferase (Gal-1-PUT), were measured in 3653 subjects aged 7 months to 84 years in der to obtain the incidence of the gene deficiency causing galactosaemia in the Western Hungarian province of Vas. To date nothing is known about these frequencies in this particular region. It was of special interest whether these enzyme defects are to be found more frequently in gypsies than in a comparable population of West Hungary. The frequency of homozygous Gal-1-PUT deficiency amounts to 1:23,500; the respective incidence of galactokinase deficiency is 1:64,000. Both enzyme deficiencies in this province are not higher than in other countries. Considerable differences were established in the gene frequencies in individual areas and for various groups of subjects with variations from 1:30,000 to 1: 127,000 for galactokinase deficiency and from 1:5,300 to 1:81,000 for Gal-1-PUT deficiency. Neither gene deficiency occurred more frequently in gypsies than in the general population. This study demonstrates that the results of such analyses are relevant only to the investigated region and the greatest possible number of subjects must be taken in order to draw reliable conclusions.

摘要

为了确定在匈牙利西部沃什州导致半乳糖血症的基因缺陷的发生率,对3653名年龄在7个月至84岁之间的受试者进行了半乳糖代谢的两种酶(即半乳糖激酶和1-磷酸半乳糖尿苷转移酶(Gal-1-PUT))的检测。迄今为止,关于这个特定地区的这些频率尚无任何信息。特别令人感兴趣的是,这些酶缺陷在吉普赛人中是否比在匈牙利西部的可比人群中更常见。纯合子Gal-1-PUT缺乏症的频率为1:23500;半乳糖激酶缺乏症的相应发生率为1:64000。该省这两种酶缺乏症的发生率并不高于其他国家。在各个地区以及不同组别的受试者中,基因频率存在相当大的差异,半乳糖激酶缺乏症的频率在1:30000至1:127000之间,Gal-1-PUT缺乏症的频率在1:5300至1:81000之间。这两种基因缺陷在吉普赛人中出现的频率都不比普通人群高。这项研究表明,此类分析的结果仅与所调查的地区相关,并且必须纳入尽可能多的受试者才能得出可靠的结论。

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