Cardiac ion channelopathies encompass a set of inherited or acquired conditions that are
due to dysfunction in ion channels or their associated proteins, typically in the presence of …

Congenital cardiac ion channelopathies refer to a set of inherited conditions characterized
by abnormalities in the structure and/or function of ion channels, their associated proteins or …

Ion channelopathies are diseases caused by dysfunctional ion channels that may lead to
sudden death. These diseases can be either acquired or inherited. The main phenotypes …

The underlying aetiology of sudden arrhythmic death syndrome is predominantly inherited
cardiac disease, and 'channelopathies'(cardiac ion channel disease) are the most common …

The inherited arrhythmia (IA) syndromes are a group of disorders characterised by an
increased risk of sudden cardiac death (SCD), abnormal cardiac electrical function and …

Over the past two decades, our understanding of inherited primary arrhythmia syndromes
has been enriched by studies that have aimed to define the clinical characteristics and the …

Inherited arrhythmia (IA) is one of the main causes of sudden cardiac death (SCD) in young
people, and is reported to be a more prevalent cause of SCD in Asia than in Western …

In spite of their relative rarity, inheritable arrhythmias have come to the forefront as a group
of potentially fatal but preventable cause of sudden cardiac death in children and (young) …

Channelopathies are diseases caused by dysfunctional ion channels, due to either genetic
or acquired pathological factors. Inherited cardiac arrhythmic syndromes are among the …

Long QT syndrome, short QT syndrome, Brugada syndrome and catecholaminergic
polymorphic ventricular tachycardia are inherited primary electrical disorders that …