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Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a chronic, progressive, heritable cardiomyopathy, characterized by fibrofatty replacement and dysfunction of right ventricular. The first symptoms of ARVC/D include palpitations, effort-induced syncope, dyspnea, chest pain, whereas sudden cardiac death is the first clinical manifestation during physical activity, training or just after physical activity in 10% of cases. It is one of the most common causes of sudden cardiac death in young athletes, accounting for approximately 22% of cases.

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