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窦房结疾病的常染色体显性遗传。

Autosomal dominant inheritance of sinus node disease.

作者信息

Lorber A, Maisuls E, Palant A

出版信息

Int J Cardiol. 1987 May;15(2):252-6. doi: 10.1016/0167-5273(87)90324-x.

Abstract

A family with sinus node disease is presented. The mother was severely affected by sinus bradycardia and required a permanent atrial pacing system. The father is asymptomatic and has no evidence of conduction disturbances. All their offspring (one son and two daughters) are affected with variable degrees of severity. The occurrence of the disease in this family is suggestive of autosomal dominant inheritance with variable penetrance.

摘要

本文介绍了一个患有窦房结疾病的家族。母亲受严重窦性心动过缓影响,需要永久性心房起搏系统。父亲无症状,无传导障碍证据。他们所有的后代(一个儿子和两个女儿)都受到不同程度的影响。该疾病在这个家族中的出现提示为具有可变外显率的常染色体显性遗传。

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