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An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK, high risk of VENTRICULAR TACHYCARDIA or VENTRICULAR FIBRILLATION, SYNCOPAL EPISODE, and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit.
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Authors: V Probst, C Veltmann, L Eckardt, P G Meregalli, F Gaita, H L Tan, D Babuty, F Sacher, C Giustetto, E Schulze-Bahr,…
Circulation 2010 Feb 9Authors: P D Lambiase, A K Ahmed, E J Ciaccio, R Brugada, E Lizotte, S Chaubey, Ron Ben-Simon, A W Chow, M D Lowe, W J McKenna
Circulation 2009 Jul 14Thought leaders and organizations working on research involving brugada syndrome.
conditions: Brugada Syndrome
interventions: 3,4-Di-amino-Pyridine ; placebo
conditions: Brugada Syndrome
interventions: hydroquinidine ; placebo (sugar)
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