Brugada syndrome 2

A Brugada syndrome that has_material_basis_in heterozygous mutation in the GPD1L gene on chromosome 3p22.

Signs and symptoms

• Prolonged PR interval
• Ventricular fibrillation
• First degree atrioventricular block
• Complete right bundle branch block
• Syncope
• Sudden cardiac death

Also known as: BRGDA2