The Brugada Syndrome (BrS) is a rare autosomal dominant genetic disease. The disease has a normal heart structure, but once the onset will have serious consequences, the main clinical manifestations are cardiogenic syncope, sudden death without organic heart disease, and the electrocardiogram is characterized by the V1~V3ST segment in a cape shape or saddle shape elevated. BrS has a tendency to cause sudden death due to rapid polymorphic ventricular tachycardia and ventricular fibrillation. Brugada Syndrome https://acroscell.creative-bioarray.com/platform/brugada-syndrome.html
