What can be done when asymptomatic patients discover they have Brugada syndrome? A case report of Brugada syndrome

被引:3
|
作者
Doetzer, Andrea Duarte [1 ]
Sotomaior, Vanessa Santos [1 ]
Bubna, Marcos Henrique [4 ]
Raskin, Salmo [1 ,2 ,3 ]
机构
[1] Pontificia Univ Catolica Parana PUCPR, Ctr Hlth & Biol Sci, Curitiba, Parana, Brazil
[2] Genetika, Lab Genet Counseling, Curitiba, Parana, Brazil
[3] Genetika, Ctr Genet Counseling, Curitiba, Parana, Brazil
[4] Hosp Cardiol Costantini Curitiba, Curitiba, Parana, Brazil
关键词
Brugada syndrome; SCN5A mutation; Cardiac disease;
D O I
10.1016/j.ijcard.2010.02.037
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Brugada syndrome is an inherited cardiac disorder associated with a specific electrocardiographic pattern, involving ST segment elevation in leads V1 to V3. When not spontaneously terminated, it can lead to ventricular fibrillation and sudden death. We present a case report of a young male whose brother suffered a sudden cardiac arrest while playing soccer. A novel mutation c.2678G>A was detected on the gene SCN5A through molecular diagnosis. The mutation was shown to be present in the individual, his daughter and his other brother. For patients with previous ventricular fibrillation and/or syncope, implantable cardiac device (ICD) is recommended. However, how can patients without symptoms but with a clear diagnosis prevent cardiac arrest? (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:E96 / E97
页数:2
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