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帕陶氏综合征(13三体综合征)的产前诊断,包括对胎儿进行详细的病理研究。

Antenatal diagnosis of Patau's syndrome (trisomy 13) including a detailed pathological study of the fetus.

作者信息

Butler L J, Reiss H E, France N E, Briddon S

出版信息

J Med Genet. 1973 Dec;10(4):367-70. doi: 10.1136/jmg.10.4.367.

Abstract

The first ever antenatal diagnosis of Patau's syndrome (trisomy 13) during the 19th week of the pregnancy of a 42-year-old woman is reported. Karyotypes were obtained from amniotic fluid cell cultures established at 17 weeks and the results were confirmed by chromosome banding studies and fetal skin cultures. The pregnancy was terminated by hysterotomy and sterilization was performed at the same operation. A detailed description of the fetus is included and the pathogenesis of arrhinencephaly is discussed. The current status of antenatal screening for chromosome anomalies is presented.

摘要

报道了一例42岁女性妊娠19周时首次产前诊断出帕陶氏综合征(13三体)的病例。通过对17周时建立的羊水细胞培养获得核型,并经染色体显带研究和胎儿皮肤培养证实结果。通过子宫切开术终止妊娠,并在同一次手术中进行绝育。文中包含了对胎儿的详细描述,并讨论了无脑畸形的发病机制。还介绍了目前染色体异常产前筛查的现状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27fb/1013058/4638533cbb1e/jmedgene00325-0060-a.jpg

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