Brugada综合征于1992年由西班牙Brugada兄弟首先报道[1]。该综合征多见于东南亚地区无心脏结构异常的年轻男性,其发病与心脏钠通道基因SCN5A突变有关,患者有心室颤动发作,可致猝死。近年来引起广泛关注。为提高对Bru-gada综合征认识,本文对该综合征的临床特征和诊治作一综述。1 Brugada syndrome was first reported in 1992 by the Brugada brothers in Spain [1]. The syndrome more common in Southeast Asia without cardiac structural abnormalities in young men, the incidence of cardiac sodium channel gene SCN5A mutation related to patients with ventricular fibrillation attack, can cause sudden death. In recent years, aroused widespread concern. In order to improve the understanding of Bru-gada syndrome, this article reviews the clinical features and diagnosis and treatment of this syndrome. 1