Brugada syndrome - A decade of progress

被引:153
作者
Antzelevitch, C
Brugada, P
Brugada, J
Brugada, R
Shimizu, W
Gussak, I
Riera, ARP
机构
[1] Masonic Med Res Lab, Utica, NY 13501 USA
[2] Onze Lieve Vrouw Hosp, Ctr Cardiovasc, Aalst, Belgium
[3] Univ Barcelona, Hosp Clin, Cardiovasc Inst, E-08007 Barcelona, Spain
[4] eResearchtechnol Inc, Bridgewater, NJ USA
[5] Natl Cardiovasc Ctr, Osaka, Japan
[6] Neomater Hosp, Hemodynam Lab, Serv Cardiol, Sao Paulo, Brazil
关键词
ventricular tachycardia; ventricular fibrillation; arrhythmia; sudden death;
D O I
10.1161/01.RES.0000046046.53721.90
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The Brugada syndrome has gained wide recognition throughout the world and today is believed to be responsible for 4% to 12% of all sudden deaths and approximate to20% of deaths in patients with structurally normal hearts. The incidence of the disease is on the order of 5 per 10 000 inhabitants and, apart from accidents, is the leading cause of death of men under the age of 50 in regions of the world where the inherited syndrome is endemic. This minireview briefly summarizes the progress made over the past decade in our understanding of the clinical, genetic, cellular, ionic, and molecular aspects of this disease.
引用
收藏
页码:1114 / 1118
页数:5
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