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Ventricular Arrhythmias in Arrhythmogenic Right Ventricular Dysplasia [PDF]
Indian Pacing and Electrophysiology Journal, 2015 In this issue of 'EP Update' we summarize the recent literature on arrhythmogenic right ventricular dysplasia (ARVD). The articles have been hand picked and reviewed by the editors of IPEJ for the benefit of readers.
Johnson Francis, MD, DM, FACC, FRCP Edin, FRCP London +1 more
doaj +4 more sources
Arrhythmogenic right ventricular cardiomyopathy/dysplasia [PDF]
Orphanet Journal of Rare Diseases, 2007 Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a heart muscle disease clinically characterized by life-threatening ventricular arrhythmias. Its prevalence has been estimated to vary from 1:2,500 to 1:5,000.
Basso Cristina +2 more
doaj +3 more sources
Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders [PDF]
Clinical Medicine Insights: Cardiology, 2016 Objectives Arrhythmogenic right ventricular dysplasia (ARVD) is a rare, genetic disorder predominantly affecting the right ventricle. There is increasing evidence that in some cases, ARVD is due to mutations in genes, which have also been implicated in ...
Josef Finsterer, Claudia Stöllberger
doaj +3 more sources
Clinical features and arrhythmic complications of patients with pediatric-onset arrhythmogenic right ventricular dysplasia [PDF]
Anatolian Journal of Cardiology, 2019 Objective: Arrhythmogenic right ventricular dysplasia (ARVD) is a myocardial genetic disease that occurs primarily in the right ventricle. Patients with ARVD may present with severe ventricular arrhythmias, syncope, and cardiac arrest.
Fatma Sevinç Şengül +6 more
doaj +2 more sources
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2019 Background It has been suggested that endocardial and epicardial ablation of ventricular tachycardia (VT) improves outcome in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Shibu Mathew +18 more
doaj +3 more sources
Implantable Cardioverter‐Defibrillator Therapy in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Predictors of Appropriate Therapy, Outcomes, and Complications [PDF]
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2017 BackgroundArrhythmogenic right ventricular dysplasia/cardiomyopathy is characterized by ventricular arrhythmias and sudden cardiac death. Once the diagnosis is established, risk stratification to determine whether implantable cardioverter‐defibrillator ...
Gabriela M. Orgeron +11 more
doaj +2 more sources
Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia
Indian Pacing and Electrophysiology Journal, 2003 Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is characterized by the patchy replacement of myocardium by fatty or fibrofatty tissue.
Julia H. Indik, Frank I. Marcus
doaj +2 more sources
A Prenatal Case of Arrhythmogenic Right Ventricular Dysplasia [PDF]
Arquivos Brasileiros de Cardiologia, 2018 Lilian Maria Lopes +4 more
doaj +2 more sources
Arrhythmogenic right ventricular dysplasia
Revista Cubana de Cardiología y Cirugía Cardiovascular, 2011 The arrhythmogenic right ventricular dysplasia is a genetic base cardiomyopathy, characterizedby the substitution of the miocardic tissue by an adipose or a fibroadipose one.
Marleny Cruz Cardentey +1 more
doaj +1 more source
Arrhythmogenic Right Ventricular Dysplasia [PDF]
Annual Review of Medicine, 1999 Arrhythmogenic right ventricular dysplasia (ARVD) is a new form of cardiomyopathy probably more frequent than commonly reported. It is a rare but important cause of sudden arrhythmic death in young, otherwise healthy persons, as well as a subtle cause of congestive heart failure.
G, Fontaine +6 more
+7 more sources