首页> 外文期刊>Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society >A high frequency of the Cystic Fibrosis 2184insA mutation in Western Ukraine: genotype-phenotype correlations, relevance for newborn screening and genetic testing.
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A high frequency of the Cystic Fibrosis 2184insA mutation in Western Ukraine: genotype-phenotype correlations, relevance for newborn screening and genetic testing.

机译:乌克兰西部的囊性纤维化2184insA突变的高频率:基因型与表型的相关性,与新生儿筛查和基因检测的相关性。

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摘要

We present the first comprehensive report on the distribution and genotype-phenotype correlations of CF-causing mutations in Western Ukraine (former Galicia). The 2184insA mutation was identified in 17 unrelated CF patients, 2 of whom are homozygotes for this allele. This mutation is associated with the classical form of CF. The high frequency of 2184insA mutation (7.20% of all mutated CF chromosomes) suggests that it is likely of Galician origin, from where it has spread throughout Europe and beyond. The achieved 83.71% mutation detection rate fulfills the minimal pre-requisite for introduction of the two-tier
机译:我们目前在乌克兰西部(前加利西亚)引起CF的突变的分布和基因型与表型的相关性上发表了第一份综合报告。在17名无关的CF患者中鉴定出2184insA突变,其中2名是该等位基因的纯合子。这种突变与CF的经典形式有关。 2184insA突变的高频率(占所有突变CF染色体的7.20%)表明,它很可能是加利西亚人起源的,从那里传播到整个欧洲及其他地区。达到83.71%的突变检测率满足引入两级检测的最低前提条件

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