Key result
Familial arrhythmogenic syndromes (channelopathies) causing sudden cardiac death in young individuals are characterized by incomplete penetrance and variable expressivity.
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This review emphasizes the importance of understanding genetic and non-genetic modifiers in channelopathies to improve early identification of individuals at risk for sudden cardiac death.
Sudden cardiac death is defined as an unexpected decease of cardiac origin. In individuals under 35 years old, most of these deaths are due to familial arrhythmogenic syndromes of genetic origin, also known as channelopathies. These familial cardiac syndromes commonly follow an autosomal dominant pattern of inheritance. Diagnosis, however, can be difficult, mainly due to incomplete penetrance and variable expressivity, which are hallmarks in these syndromes. The clinical manifestation of these diseases can range from asymptomatic to syncope but sudden death can sometimes be the first symptom of disease. Early identification of at-risk individuals is crucial to prevent a lethal episode. In this review, we will focus on the genetic basis of channelopathies and the effect of genetic and non-genetic modifiers on their phenotypes.
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Coll et al. (2017) conducted a review in Channelopathies associated with sudden cardiac death. Genetic and non-genetic modifiers was evaluated. Familial arrhythmogenic syndromes (channelopathies) causing sudden cardiac death in young individuals are characterized by incomplete penetrance and variable expressivity.
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