Late-onset severe long QT syndrome

被引：1

作者：

Asatryan, Babken ^{[1
]}

Schaller, Andre ^{[2
]}

Bartholdi, Deborah ^{[2
]}

Medeiros-Domingo, Argelia ^{[1
]}

机构：

[1] Univ Bern, Bern Univ Hosp, Univ Clin Cardiol, Inselspital, Bern, Switzerland

[2] Univ Bern, Bern Univ Hosp, Dept Pediat, Inselspital,Div Human Genet, Bern, Switzerland

来源：

ANNALS OF NONINVASIVE ELECTROCARDIOLOGY | 2018年 / 23卷 / 04期

关键词：

channelopathy; genetic test; long QT syndrome; sudden death; SUDDEN CARDIAC DEATH; POTASSIUM CHANNEL; PROLONGATION; MUTATIONS; VARIANTS; GENETICS; SEX; AGE;

D O I：

10.1111/anec.12517

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

We report a case of torsades de pointes arrhythmia as the first manifestation of congenital Long QT syndrome in a 77-year-old man with family history of sudden unexplained death. This case illustrates the importance of vigilant clinical assessment and genetic counseling in families with sudden death in order to identify properly asymptomatic relatives at risk for cardiac events. It also demonstrates that Long QT syndrome can still manifest with potentially fatal arrhythmias late in life in previously asymptomatic elderly patients.

引用

页数：5

共 19 条

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