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遗传性束支系统缺陷。一种新的遗传实体?

Hereditary bundle branch system defect. A new genetic entity?

作者信息

Stéphan E

出版信息

Am Heart J. 1979 Jun;97(6):708-18. doi: 10.1016/0002-8703(79)90005-x.

Abstract

A familial survey demonstrated mendelian inheritance in three large kindreds with conduction abnormalities and heart block. The trait was autosomal dominant, with varying expressivity and penetrance, apparent male preponderance, and congenital onset. Manifestations included right bundle branch block, left axis deviation, and right bundle branch block associated with left axis deviation. Complete heart block proved almost always to be a late event, and developed in all documented cases from bilateral bundle branch block. An r' pattern, most likely representing a right ventricular conduction delay, is discussed.

摘要

一项家族调查显示,在三个患有传导异常和心脏传导阻滞的大型家族中存在孟德尔遗传。该性状为常染色体显性遗传,具有不同的表现度和外显率,明显男性居多,且为先天性发病。表现包括右束支传导阻滞、左轴偏移以及与左轴偏移相关的右束支传导阻滞。完全性心脏传导阻滞几乎总是晚期出现,并且在所有有记录的病例中均由双侧束支传导阻滞发展而来。文中讨论了一种最有可能代表右心室传导延迟的r'波型。

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