Molecular Insight: Brugada Syndrome

Baig, Atif Amin and Ahmad Sheikh , Shabbir and Simbak, Nordin and Alwi, Zilfalil (2013) Molecular Insight: Brugada Syndrome. 1, 1 (1). LULU, USA. ISBN 9781304656438

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Abstract

Brugada’s syndrome (BrS) is a cardiac disease with an autosomal dominant pattern of inheritance. The syndrome is characterized by syncopal episodes and/or sudden death in patients with a structurally normal heart and characterized by ST-segment elevation in the right precordial leads (V1–V3) of the electrocardiogram (ECG). There is propensity for sudden death due to rapid polymorphic ventricular tachycardia (VT) or ventricular fibrillation (VF). This mini booklet will be useful for undergraduate students to understand the Brugada syndrome and underlaying molecular cause.

Item Type: Book
Subjects: R Medicine > R Medicine (General)
Faculty / Institute: Faculty of Medicine
Depositing User: Dr Atif Baig
Date Deposited: 07 Jan 2015 02:39
Last Modified: 27 Apr 2015 08:02
URI: http://erep.unisza.edu.my/id/eprint/1806

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