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[囊性纤维化携带者筛查。一项针对孕妇的试点研究结果]

[Screening for carriers of cystic fibrosis. Result of a pilot study among pregnant women].

作者信息

Brandt N J, Schwartz M, Skovby F

机构信息

Afsnit for klinisk genetik, Rigshospitalet, København.

出版信息

Ugeskr Laeger. 1994 Jun 20;156(25):3751-4, 3757.

PMID:8059452
Abstract

Total prevention of cystic fibrosis (CF) is possible if all carrier women are found before pregnancy or early enough during pregnancy so that prenatal diagnosis can be offered. The delta 508 allele constitutes almost 90% of the mutations causing CF in the Danish population. We have examined 6599 pregnant women and found 172 carriers of delta F508. Partners of carrier women were examined for delta F508 and five other mutations. Three couples at risk and one foetus with CF were identified. Giving information to couples before and after testing is time consuming. A comprehensive questionnaire was sent to 200 non-carriers and all 172 carriers (response rate 72%). It can be concluded that the project has been very well accepted. However, the majority of carriers were shocked or very worried when they had the test result. Based on this pilot study we recommend nationwide screening for delta F508 early in pregnancy.

摘要

如果能在所有携带致病基因的女性怀孕前或孕期足够早的时候就检测出来,以便进行产前诊断,那么完全预防囊性纤维化(CF)是有可能的。在丹麦人群中,Δ508等位基因几乎构成了导致CF的90%的突变。我们检查了6599名孕妇,发现了172名携带ΔF508的携带者。对携带致病基因女性的伴侣进行了ΔF508及其他五种突变的检测。确定了三对有风险的夫妇和一名患有CF的胎儿。在检测前后向夫妇提供信息很耗时。向200名非携带者和所有172名携带者发送了一份综合问卷(回复率72%)。可以得出结论,该项目得到了很好的接受。然而,大多数携带者在得知检测结果时感到震惊或非常担忧。基于这项初步研究,我们建议在全国范围内对孕期早期的ΔF508进行筛查。

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