Open AccessA clinical case of arrhythmogenic right ventricular dysplasia
Author(s) -
Е. В. Соловьева,
Н А Попова,
Т. В. Власова,
Maria Gorbunova,
L N Antsygina
Publication year - 2021
Publication title -
ûžno-rossijskij žurnal terapevtičeskoj praktiki
Language(s) - English
Resource type - Journals
ISSN - 2712-8156
DOI - 10.21886/2712-8156-2021-2-1-109-114
Subject(s) - asymptomatic , arrhythmogenic right ventricular dysplasia , medicine , cardiology , dysplasia , disease , sudden cardiac death , sudden death , cardiomyopathy , heart failure
Arhythmogenic right ventricular dysplasia (ADP) refers to hereditary myocardial diseases, in which there are structural and functional disorders in the right ventricular myocardium, causing rhythm and conduction disorders, including fatal ventricular arrhythmias. ADP is considered one of the most common causes of sudden cardiac death in young people and people who are engaged in sports. However, in practice, there are cases of this disease in people of an older age category. Diagnosis of ADP is still difficult due to the possible long-term asymptomatic course of the disease. The article describes a clinical case of ADP in a 48-year-old man.