Results 21 to 30 of about 14,748 (188)

Evolving Diagnostic Criteria for Arrhythmogenic Cardiomyopathy

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2021
Criteria for diagnosis of arrhythmogenic cardiomyopathy (ACM) were first proposed in 1994 and revised in 2010 by a Task Force. Although the Task Force criteria demonstrated a good accuracy for diagnosis of the original right ventricular phenotype ...
Domenico Corrado, Alessandro Zorzi, Alberto Cipriani, Barbara Bauce, Riccardo Bariani, Giorgia Beffagna, Manuel De Lazzari, Federico Migliore, Kalliopi Pilichou, Alessandra Rampazzo, Ilaria Rigato, Stefania Rizzo, Gaetano Thiene, Martina Perazzolo Marra, Cristina Basso   +14 more
doaj   +1 more source

Familial screening in case of acute myocarditis reveals inherited arrhythmogenic left ventricular cardiomyopathies

ESC Heart Failure, 2020
Aims Several data suggest that acute myocarditis could be related to genetic variants involved in familial cardiomyopathies, particularly arrhythmogenic cardiomyopathy, but the management of patients with acute myocarditis and their families regarding ...
Nicolas Piriou, Lara Marteau, Florence Kyndt, Jean Michel Serfaty, Claire Toquet, Laurianne Le Gloan, Karine Warin‐Fresse, Damien Guijarro, Thierry Le Tourneau, Emilie Conan, Aurélie Thollet, Vincent Probst, Jean‐Noël Trochu   +12 more
doaj   +1 more source

Focus on arrhythmogenic right ventricular cardiomyopathy [PDF]

European Heart Journal Supplements, 2020
Abstract Arrhythmogenic right ventricular cardiomyopathy is a myocardial disease generally caused by desmosomal mutations and characterized by progressive replacement of cardiomyocites with fibro-adipose tissue. In the classic form of the disease right ventricle is predominantly affected. However, biventricular and left-dominant variants
Sinagra G., Cappelletto C., de Luca A., Romani S., Paldino A., Korcova R., Dal Ferro M., Vitrella G., Pagnan L., Pinamonti B.   +9 more
openaire   +3 more sources

Arrhythmogenic right ventricular cardiomyopathy in monozygotic twin sisters, and persistent left superior vena cava in one complicating implantation of ICD

Türk Kardiyoloji Derneği Arşivi, 2015
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterized histologically by fibro-fatty replacement of heart muscle, and clinically by ventricular arrhythmias and right ventricular dysfunction.
Mehmet Ali Astarcıoğlu, Mehmet Yaymacı, Taner Şen, Celal Kilit, Basri Amasyalı   +4 more
doaj   +1 more source

Emergency department extracorporeal membrane oxygenation as a rescue therapy for ventricular tachycardia electrical storm: a case report

Journal of the American College of Emergency Physicians Open, 2020
Arrhythmogenic right ventricular cardiomyopathy is a cause of sudden cardiac death in often otherwise healthy young adults. Cardiac arrest following an unstable tachydysrhythmia may be the primary presenting symptom.
Andrew Pugh, Joseph E. Tonna, Scott Youngquist, John J. Ryan, Graham Brant‐Zawadzki   +4 more
doaj   +1 more source

Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy [PDF]

Circulation, 2003
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a disease characterized by fatty replacement of the right ventricular muscle (1). The residual myocardial fibers are often embedded in fibrous tissue. This substrate is conducive to right ventricular re-entrant arrhythmias. Initially this condition was called dysplasia because it was
Kathleen, Gear, Frank, Marcus
openaire   +2 more sources

Mixed phenotype cardiomyopathy, associated with DSP genetic variant: a case report and literature review.

Российский кардиологический журнал, 2020
We report a case of mixed phenotype cardiomyopathy (non-compaction cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy), associated with DSP genetic variant.  The sudden cardiac death was the first and only symptom.
I. V. Shlyk, A. A. Streltsova, V. M. Teplov, E. G. Gavrilova, A. N. Kulikov, A. N. Krutikov, M. G. Rybakova, I. A. Kuznetsova, S. E. Andreeva, T. G. Bezhanishvili, A. A. Khudiakov, A. A. Kostareva, A. Ya. Gudkova   +12 more
doaj   +1 more source

Genetics of arrhythmogenic right ventricular cardiomyopathy [PDF]

Journal of Medical Genetics, 2013
Arrhythmogenic right ventricular cardiomyopathy is a rare clinical entity characterised by fibro-fatty replacement of myocardium, mainly involving right ventricular free wall, leading to malignant electrical instability and sudden cardiac death.
Campuzano, O, Alcalde, M, Allegue, C, Iglesias, A, García Pavía, P, Partemi, Sara, Oliva, Antonio, Pascali, Vincenzo Lorenzo, Berne, P, Sarquella Brugada, G, Brugada, J, Brugada, P, Brugada, R.   +12 more
openaire   +6 more sources

Wide Complex Tachycardia in Arrhythmogenic Right Ventricular Cardiomyopathy: Electrocardiogramand Intracardiac Electrogram Features

Indian Journal of Clinical Cardiology, 2022
Case of an arrhythmogenic right ventricular cardiomyopathy with associated arrhythmias discussing classical electrocardiogram and intracardiac electrogram findings.
Rangadham Nagarakanti, Kavin Raj
doaj   +1 more source

Arrhythmogenic right ventricular cardiomyopathy

Journal of the American College of Cardiology, 2001
Arrhythmogenic right ventricular (RV) cardiomyopathy (ARVC) is a cardiomyopathy characterized pathologically by fibrofatty replacement primarily of the RV and clinically by life-threatening ventricular arrhythmias in apparently healthy young people. The prevalence of the disease has been estimated at 1 in 5,000 individuals, although this estimate will ...
Gemayel, Carol, Pelliccia, Antonio, Thompson, Paul D   +2 more
openaire   +2 more sources