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关于梅克尔综合征的信息与遗传咨询(作者译)

[Contribution to information and genetic counseling in Mekkel's syndrome (author's transl)].

作者信息

Koch G, Schwanitz G

出版信息

MMW Munch Med Wochenschr. 1975 Oct 24;117(43):1723-4.

PMID:52836
Abstract

The deformity syndrome nowadays named after Meckel is characterized by the following principal features: occipital encephalocele, cystic kidneys and a polydactyly. According to the available findings in twins and families, an autosomal recessive lethal syndrome is involved. In 8 (= 16.6%) of 48 families, the parents of the feature carrier were blood relations. Heterozygous anlage carriers cannot yet be recognized as such. To make a statement in genetic counselling today, ultrasonic diagnosis and an amniocentesis must be carried out early in a pregnancy at risk.

摘要

如今以梅克尔命名的畸形综合征具有以下主要特征

枕部脑膨出、多囊肾和多指畸形。根据双胞胎及家族中的现有发现,这是一种常染色体隐性致死综合征。在48个家族中有8个(占16.6%),特征携带者的父母是近亲。杂合子遗传基础携带者目前尚无法识别。为了在如今的遗传咨询中做出诊断,对于有风险的妊娠必须尽早进行超声诊断和羊膜穿刺术。

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