Arrhythmogenic right ventricular cardiomyopathy
Parveen Bhardwaj, Minoo Sharma, Neeraj Ganju
Abstract
Parveen Bhardwaj, Minoo Sharma, Neeraj Ganju
Abstract
Arrhythmogenic right ventricular cardiomyopathy (ARVC) also called as arrhythmogenic right ventricular dysplasia (ARVD) is an inherited heart muscle disease that predominantly affects the right ventricle (RV). The main pathologic feature is the progressive loss of RV myocardium and its replacement by fibrofatty tissue. Clinical manifestations develop most often between the second and third decades of life and are related to ventricular tachycardia (VT) or ventricular fibrillation (VF), which may lead to sudden death in young people.
OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) also called as arrhythmogenic right ventricular dysplasia (ARVD) is an inherited heart muscle disease that predominantly affects the right ventricle (RV). The main pathologic feature is the progressive loss of RV myocardium and its replacement by fibrofatty tissue. Clinical manifestations develop most often between the second and third decades of life and are related to ventricular tachycardia (VT) or ventricular fibrillation (VF), which may lead to sudden death in young people.
Key concepts: Cardiology, Arrhythmogenic right ventricular dysplasia, Medicine, Ventricle, Internal medicine, Cardiomyopathy, Ventricular tachycardia, Ventricular fibrillation