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Case Reports
An ECG changed the life of a young boy: a case of arrhythmogenic right ventricular dysplasia.
- Ibrahim Altun, Fatih Akin, Cem Sahin, and Halil Beydilli.
- Department of Cardiology, Mugla Sitki Kocman University Medical Faculty, Mugla, Turkey.
- BMJ Case Rep. 2014 Oct 24; 2014.
AbstractArrhythmogenic right ventricular dysplasia (ARVD) is a progressive condition with the right ventricular myocardium being replaced by fibrofatty tissue. It is a hereditary disorder mostly caused by desmosome gene mutations. The prevalence of arrhythmogenic right ventricular cardiomyopathy is about 1/1000-5000. Clinical presentation is usually related to ventricular tachycardias, syncope, presyncope or ventricular fibrillation leading to cardiac arrest, mostly in young people and athletes. We report a case of a 17-year-old boy from Turkey, who was referred to our cardiology department for an ECG, required of him prior to joining a football team. 2014 BMJ Publishing Group Ltd.
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