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对2例心脏性摔死获救的Brugada综合征患者及其家系中25个成员进行调查。结果除2例先征者外，家系中还有5例心电图具右束支传导阻滞伴STV1～V3抬高特征，支持Brugada综合征是一种常染色体显形遗传疾病，值得临床医生和心电图技师重视。
Two patients with Brugada syndrome who were rescued from cardiac arrest and 25 from their family were investigated. Results In addition to two cases of preemptive, there are five cases of pedigrees with right bundle branch block with STV1 ~ V3 elevation characteristics, support for Brugada syndrome is an autosomal dominant genetic disease, it is worth clinicians and ECG technicians Pay attention.