Brugada syndrome 1

A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN5A gene on chromosome 3p22.

Signs and symptoms

• Syncope
• Ventricular fibrillation
• Complete right bundle branch block
• Sudden cardiac death
• Atrial fibrillation
• Cardiac arrest
• Supraventricular tachycardia with an accessory connection mediated pathway
• Atrial flutter

Also known as: BRGDA1