SCD can occur in children, adolescents, and young adults within minutes of the onset of cardiac symptoms [9].Recent studies have found that about 30% of negative autopsies in young individuals (<15 years) could possibly be explained by pathogenic variations in channelopathies-related genes [10].Additionally, it has been found that approximately two-thirds of survivors of sudden cardiac arrest are subsequently diagnosed with a channelopathy condition [6] The most prevalent cardiac channelopathies are long QT syndrome (LQTS) [11], Brugada syndrome (BrS) [12], short QT syndrome (SQTS) [13] and catecholaminergic polymorphic ventricular tachycardia (CPVT) [14].