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家族性完全性肺静脉异位引流:一个来自犹他州和爱达荷州的大家族。

Familial total anomalous pulmonary venous return: a large Utah-Idaho family.

作者信息

Bleyl S, Ruttenberg H D, Carey J C, Ward K

机构信息

Department of Obstetrics and Gynecology, University of Utah Health Sciences Center, Salt Lake City.

出版信息

Am J Med Genet. 1994 Oct 1;52(4):462-6. doi: 10.1002/ajmg.1320520412.

Abstract

Total anomalous pulmonary venous return (TAPVR) is a rare form of cyanotic congenital heart disease which, without surgical correction, has a high mortality rate in the first year of life. It usually occurs without a family history, and is generally thought to have a low recurrence risk. However, 15 instances of familial TAPVR have been reported previously, suggesting a genetic cause in some cases. We report on a large family in which TAPVR appears to be determined multifactorially or as an autosomal dominant trait with variable expressivity and reduced penetrance.

摘要

完全性肺静脉异位回流(TAPVR)是一种罕见的青紫型先天性心脏病,若不进行手术矫正,在出生后第一年死亡率很高。该病通常无家族病史,一般认为复发风险较低。然而,此前已报道过15例家族性TAPVR病例,提示在某些情况下存在遗传因素。我们报告了一个大家庭,其中TAPVR似乎是由多因素决定的,或者是一种具有可变表达性和降低外显率的常染色体显性性状。

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