Brugada syndrome 3

info · Genetic · ICD-10: I49.8

A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the alpha-1C subunit of the L-type voltage-dependent calcium channel (CACNA1C) on chromosome 12p13.

Signs and symptoms

Shortened QT interval
J wave
Atrial fibrillation
Ventricular arrhythmia
Syncope
Sudden cardiac death

Also known as: BRGDA3