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Review outlines genetic and diagnostic work-up for congenital conditions causing SCD in children and athletes.
This review summarizes the genetic background and diagnostic work-up for sudden cardiac death in children and young athletes, highlighting the role of congenital electrical disorders and structural heart diseases.
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May aid evaluation of SCD risk in young athletes; leaves open prospective validation of genetic-structural algorithms.
Sudden cardiac death is a rare but socially devastating event. The most common causes of sudden cardiac death are congenital electrical disorders and structural heart diseases. The majority of these diseases have an incomplete penetrance and variable expression; therefore, patients may be unaware of their illness. In several cases, physical activity can be the trigger for sudden cardiac death as first symptom. Our purpose is to review the causes of sudden cardiac death in sportive children and young adults and its genetic background. Symptomatic individuals often receive an implantable cardioverter-defibrillator, the preventive treatment for sudden cardiac death in most of cases due to channelopathies, which can become a challenging option in young and active patients. The identification of one of these diseases in asymptomatic patients has similarly a great impact on their everyday life, especially on their ability to undertake competitive physical activities, and the requirement of prophylactic treatment. We review main causes of sudden cardiac death in relation to its genetics and diagnostic work-up
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Sarquella‐Brugada et al. (2012) conducted a review in Sudden cardiac death. This review outlines the genetic background and diagnostic work-up of congenital electrical disorders and structural heart diseases causing sudden cardiac death in children and young athletes.
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