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孤立性房颤是由基因决定的吗?关于家族病史

[Is isolated atrial fibrillation genetically determined? Apropos of a familial history].

作者信息

Poret P, Mabo P, Deplace C, Leclercq C, Gras D, Marec B L, Daubert C

机构信息

Service de cardiologie A, CHRU, Rennes.

出版信息

Arch Mal Coeur Vaiss. 1996 Sep;89(9):1197-1203.

PMID:8952845
Abstract

The authors report five cases of apparently lone atrial fibrillation in five members of the same family from three generations. The atrial fibrillation occurred at an early age and rapidly became permanent in all cases. With time, in the absence of complications, structural cardiac abnormalities were documented by echocardiography (biatrial dilatation and mitral and tricuspid regurgitation). These observations raise the question of genetic predisposition to lone atrial fibrillation at least in this particular clinical context.

摘要

作者报告了来自三代同一家族的五名成员发生明显孤立性心房颤动的五例病例。心房颤动均在早年发生,且在所有病例中迅速转变为永久性房颤。随着时间推移,在无并发症的情况下,超声心动图检查记录到心脏结构异常(双房扩大以及二尖瓣和三尖瓣反流)。这些观察结果至少在这种特定临床情况下引发了关于孤立性心房颤动遗传易感性的问题。

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