Brugada syndrome: Recent advances and controversies

Charles Antzelevitch, Eyal Nof

Research output: Contribution to journalReview articlepeer-review

Abstract

The Brugada syndrome, first described as a new clinical entity in 1992, is widely recognized today as a form of inherited sudden cardiac arrest. The past 16 years witnessed a progressive increase in the number of reported cases and a dramatic proliferation of articles serving to define the clinical, genetic, cellular, ionic, and molecular aspects of the disease. This article provides a brief overview of recent advances in our understanding of the clinical presentation and molecular and cellular mechanisms and an update of existing controversies.

Original languageEnglish
Pages (from-to)376-383
Number of pages8
JournalCurrent Cardiology Reports
Volume10
Issue number5
DOIs
StatePublished - 2008
Externally publishedYes

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