Suppr超能文献

膈肌缺损、肢体缺陷和颅骨骨化缺陷:一种独特的畸形综合征。

Diaphragmatic defects, limb deficiencies, and ossification defects of the skull: a distinctive malformation syndrome.

作者信息

Froster U G, Kolditz P, Wisser J, Robbiani M B, Stallmach T, Hebisch G, Huch R, Huch A

机构信息

Department of Obstetrics and Gynecology, University Hospital, Zürich, Switzerland.

出版信息

Am J Med Genet. 1996 Mar 1;62(1):48-53. doi: 10.1002/(SICI)1096-8628(19960301)62:1<48::AID-AJMG10>3.0.CO;2-V.

Abstract

We report on prenatal and postnatal findings in 4 consecutive fetuses with a pattern of severe congenital anomalies who were born to a healthy nonconsanguineous couple. The spectrum of malformations includes diaphragmatic defects, hypoplastic lungs, omphalocele, limb deficiencies, syndactyly of toes, and ossification defects of the skull. This specific spectrum of anomalies is not fully compatible with that of any established syndrome. No prenatal exposure to any possible teratogen was found. Family history is suggestive for autosomal recessive inheritance, even though germ-line mosaicism in one of the parents cannot completely be excluded.

摘要

我们报告了4例连续出生的胎儿的产前和产后检查结果,这些胎儿患有严重先天性畸形,其父母为健康的非近亲夫妇。畸形谱包括膈缺损、肺发育不全、脐膨出、肢体缺如、并趾畸形以及颅骨骨化缺陷。这种特定的畸形谱与任何已确定的综合征均不完全相符。未发现产前接触任何可能致畸剂的情况。家族史提示为常染色体隐性遗传,尽管不能完全排除父母一方存在生殖系嵌合体的可能性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验