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家族性窦房结与房室传导联合功能障碍

Familial combined sinus node and atrioventricular conduction dysfunctions.

作者信息

Barak M, Herschkowitz S, Shapiro I, Roguin N

出版信息

Int J Cardiol. 1987 May;15(2):231-9. doi: 10.1016/0167-5273(87)90319-6.

Abstract

Eighteen members of a family were investigated for cardiac conduction abnormalities following the discovery of a second-degree atrioventricular block in a fetus at 35 weeks of gestation. The conduction disturbance was diagnosed by ultrasonography. Seven of the family members were diagnosed as suffering from sinus node dysfunction and/or various degrees of atrioventricular block. Three of them were children aged 9 months to 6 years and all were asymptomatic. The symptomatic family members were two adults. One of them had a pacemaker inserted for a complete atrioventricular block and Adam-Stokes attacks while the other had had several fainting attacks. The clinical, electrocardiographic and ultrasonographic findings of the family members are presented. Previous reports in literature have documented the dominant transmission of familial sinus node dysfunctions or of familial cardiac conduction disturbances. The coexistence of both dysfunctions in the same family has not been emphasized in previous reports. A review of these previously reported families, as well as our patients, suggests the need of investigation and follow-up of the families in which one member of any age is diagnosed as suffering from an "idiopathic" disturbance of the cardiac conduction system.

摘要

在一名妊娠35周胎儿被诊断为二度房室传导阻滞之后,对一个家族的18名成员进行了心脏传导异常方面的调查。这种传导障碍通过超声检查得以诊断。该家族中有7名成员被诊断患有窦房结功能障碍和/或不同程度的房室传导阻滞。其中3名是年龄在9个月至6岁的儿童,均无症状。有症状的家族成员为两名成年人。其中一人因完全性房室传导阻滞和阿-斯综合征发作而植入了起搏器,另一人则有过几次晕厥发作。文中呈现了这些家族成员的临床、心电图和超声检查结果。文献中先前的报道记录了家族性窦房结功能障碍或家族性心脏传导障碍的显性遗传。同一家庭中这两种功能障碍并存的情况在先前的报道中未得到强调。对这些先前报道的家族以及我们的患者进行回顾后发现,对于任何年龄的成员被诊断患有“特发性”心脏传导系统障碍的家族,都有必要进行调查和随访。

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