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- W2000465057 abstract "The Brugada syndrome is a genetically determined disease caused by mutations of the cardiac sodium channel. The disease affects mainly males in their forties and causes sudden cardiac death because of polymorphic ventricular tachycardia. These patients have a structurally normal heart. The electrocardiogram of this syndrome shows, spontaneously or after Class 1 antiarrhythmic drugs, ST segment elevation in leads V1 to V3 and a pattern resembling a right bundle branch block. Phase 2 reentry between epi- and endocardiac layers is responsible for the arrhythmias. The only effective treatment at present is implantation of a cardioverter defibrillator. A.N.E. 2000;5(1):88–91" @default.
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- W2000465057 date "2000-01-01" @default.
- W2000465057 modified "2023-09-22" @default.
- W2000465057 title "The Brugada Syndrome" @default.
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- W2000465057 doi "https://doi.org/10.1111/j.1542-474x.2000.tb00251.x" @default.
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