Brugada Syndrome: Case Report and Overview

被引：0

作者：

Yuce, Murat ^{[1
]}

Yavuz, Fethi ^{[1
]}

Cakici, Musa ^{[1
]}

Sari, Ibrahim ^{[1
]}

Yildirim, Cuma ^{[2
]}

Al, Behcet ^{[2
]}

Davutoglu, Vedat ^{[1
]}

机构：

[1] Gaziantep Univ, Tip Fak, Kardiyoloji Anabilim Dali, Gaziantep, Turkey

[2] Gaziantep Univ, Tip Fak, Acil Tip Anabilim Dali, Gaziantep, Turkey

来源：

EURASIAN JOURNAL OF EMERGENCY MEDICINE | 2012年 / 11卷 / 04期

关键词：

Brugada syndrome; ECG; theraphy;

D O I：

10.5152/jaem.2011.054

中图分类号：

R4 [临床医学];

学科分类号：

1002 ; 100602 ;

摘要：

Brugada syndrome is an autosomal dominant geneticl disease which is characterised by abnormal ECG and risk of sudden cardiac death. A typical finding of this syndrome is the presence of ST segment elevation in precordial V1, V2 and V3 leads with concomitant right bundle branch block on ECG. We observed that misdiagnosis or difficulty in diagnosis are generally encountered in routine clinical practice for Brugada syndrome. Herein we would like to share a typical case and overview of Brugada syndrome in the context of the latest published literature.

引用

页码：245 / 248

页数：4

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