Arrhythmogenic right ventricular cardiomyopathy

Summary Arrhythmogenic right ventricular cardiomyopathy is a rare inherited heart-muscle disease that is a cause of sudden death in young people and athletes. Causative mutations in genes encoding desmosomal proteins have been identified and the disease is nowadays regarded as a genetically determin...

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Veröffentlicht in:	The Lancet (British edition) 2009-04, Vol.373 (9671), p.1289-1300
Hauptverfasser:	Basso, Cristina, MD, Corrado, Domenico, MD, Marcus, Frank I, Prof, Nava, Andrea, MD, Thiene, Gaetano, Prof
Format:	Artikel
Sprache:	eng
Schlagworte:	Adrenergic beta-Antagonists - therapeutic use Aftercare Anti-Arrhythmia Agents - therapeutic use Apoptosis Arrhythmogenic Right Ventricular Dysplasia - diagnosis Arrhythmogenic Right Ventricular Dysplasia - epidemiology Arrhythmogenic Right Ventricular Dysplasia - genetics Arrhythmogenic Right Ventricular Dysplasia - therapy Athletes Biological and medical sciences Biopsy Cardiac arrhythmia Cardiac dysrhythmias Cardiology. Vascular system Causality Cause of Death Cell adhesion & migration Death, Sudden, Cardiac - etiology Death, Sudden, Cardiac - prevention & control Defibrillators, Implantable Disease Progression Drugs Dystrophy Early Diagnosis Electrocardiography General aspects Genes Genetic Carrier Screening Genetic screening Genetic Testing Heart Humans Internal Medicine Medical sciences Mutation Myocytes, Cardiac - ultrastructure Rare Diseases Risk Assessment Risk factors Sensitivity and Specificity
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