Suppr超能文献

伴有可能常染色体隐性遗传的严重脑和肢体缺陷:六例病例系列及文献复习

Severe brain and limb defects with possible autosomal recessive inheritance: a series of six cases and review of the literature.

作者信息

Labrune P, Trioche P, Fallet-Bianco C, Roume J, Narcy F, Le Merrer M

机构信息

Service de Pédiatrie, Hôpital Antoine Béclère, Clamart, France.

出版信息

Am J Med Genet. 1997 Dec 12;73(2):144-9.

PMID:9409864
Abstract

Six fetuses with normal chromosomes were found to have severe craniofacial, limb, and visceral malformations during the second trimester of pregnancy. Two of these fetuses were monozygotic twins while a third one had a healthy dizygotic twin brother. A case with familial recurrence was also observed. Autopsy and skeletal radiographs suggested several diagnoses such as neural tube defect with limb defects or XK aprosencephaly. The development of these severe conditions in monozygotic twins and familial recurrence emphasize the difficulties of genetic counseling in such situations. These cases may suggest autosomal recessive inheritance.

摘要

在妊娠中期发现6例染色体正常的胎儿存在严重的颅面、肢体和内脏畸形。其中2例胎儿为单卵双胞胎,另一例有一个健康的双卵双胞胎兄弟。还观察到1例有家族复发情况。尸检和骨骼X光片提示了几种诊断,如伴有肢体缺陷的神经管缺陷或无脑回畸形。单卵双胞胎中这些严重病症的发生以及家族复发情况凸显了在此类情况下进行遗传咨询的困难。这些病例可能提示常染色体隐性遗传。

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