| Literature DB >> 25344388 |
Ibrahim Altun1, Fatih Akin1, Cem Sahin2, Halil Beydilli3.
Abstract
Arrhythmogenic 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.Entities:
Mesh:
Year: 2014 PMID: 25344388 PMCID: PMC4212196 DOI: 10.1136/bcr-2014-204703
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X