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摘要： 回顾在遗传性心律失常领域最新发表的相关研究，主要关注与儿童心源性猝死关系密切的离子通道病，包括长QT综合征（LQTS）、短QT综合征（SQTS）、Brugada综合征（BrS）和儿茶酚胺敏感性多形性室性心动过速（CPVT），总结它们在发病机制及诊治方面的进展。
关键词: 心律失常, , 心性 , Brugada综合征, 心动过速, , 室性, 猝死, , 心脏, 婴儿猝死
Abstract: Recent and relevant research published in the field of inherited arrhymias were reviewed, focusing on the 'channelopathies' that are associated with sudden cardiac death (SCD) in children, including long QT syndrome (LQTS), short QT syndrome (SQTS), Brugada syndrome(BrS), and catecholaminergic polymorphic ventricular tachycardia (CPVT).
Key words: arrhythmias, , cardiac, brugada syndrome; , tachycardia, , ventricular, death, , sudden, , cardiac, sudden infant death
冯琳1，张秀芳2. 儿童遗传性心律失常的诊治进展[J]. 临床荟萃, doi: 10.3969/j.issn.1004-583X.2019.03.003.
Feng Lin1, Zhang Xiufang2. Progress of inherited arrhythmia in children[J]. Clinical Focus, doi: 10.3969/j.issn.1004-583X.2019.03.003.
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链接本文: https://huicui.hebmu.edu.cn/CN/10.3969/j.issn.1004-583X.2019.03.003
https://huicui.hebmu.edu.cn/CN/Y2019/V34/I3/207
