Results 11 to 20 of about 26,419 (210)

Arrhythmogenic right ventricular cardiomyopathy [PDF]

The Lancet, 2009
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 determined myocardial dystrophy.
BASSO, CRISTINA, CORRADO, DOMENICO, MARCUS FI, NAVA, ANDREA, THIENE, GAETANO   +4 more
exaly   +9 more sources

Arrhythmogenic right ventricular cardiomyopathy [PDF]

Journal of Arrhythmia, 2018
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a progressive cardiomyopathy characterized by fibrofatty infiltration of the myocardium, ventricular arrhythmias, sudden death, and heart failure. ARVC may be an important cause of syncope, sudden
Yongkeun Cho
doaj   +3 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, Corrado Domenico, Thiene Gaetano   +2 more
doaj   +3 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

Arrhythmogenic Right Ventricular Cardiomyopathy

JACC: Clinical Electrophysiology, 2022
Arrhythmogenic right ventricular cardiomyopathy (ARVC) encompasses a group of conditions characterized by right ventricular fibrofatty infiltration, with a predominant arrhythmic presentation. First described in the late 1970s and early 1980s, it is now frequently recognized to have biventricular involvement.
Andrew D, Krahn, Arthur A M, Wilde, Hugh, Calkins, Andre, La Gerche, Julia, Cadrin-Tourigny, Jason D, Roberts, Hui-Chen, Han   +6 more
  +9 more sources

Arrhythmogenic Right Ventricular Cardiomyopathy [PDF]

Circulation: Arrhythmia and Electrophysiology, 2011
Arrhythmogenic disorders of genetic origin include structural cardiomyopathies and inherited arrhythmic syndromes.1 Arrhythmogenic right ventricular cardiomyopathy (ARVC) is listed among the former, because it is characterized by structural and functional abnormalities of the right ventricle (RV), ranging from regional wall motion abnormalities and ...
PILICHOU, KALLIOPI, THIENE, GAETANO, Corrado D, BASSO, CRISTINA   +3 more
  +11 more sources

Arrhythmogenic Right Ventricular Cardiomyopathy: Diagnosis, Risk Stratification, and Treatment. [PDF]

Dtsch Arztebl Int
Kreimer F, Saguner AM, Akin I, Milting H, Eckardt L, El-Battrawy I.   +5 more
europepmc   +3 more sources

Arrhythmogenic right ventricular cardiomyopathy [PDF]

Heart, 2004
These are the images of a previously fit 24 year old man who was found struggling for breath. He collapsed and died. He had no significant past medical history, and there was no family …
A S, John, R H, Mohiaddin, M N, Sheppard
openaire   +2 more sources

Biventricular arrhythmogenic cardiomyopathy diagnosed in a young patient: A case report with literature review

Radiology Case Reports, 2023
Arrhythmogenic cardiomyopathy is a genetic heart muscle disease that typically affects the right ventricle. However, 2 other phenotypes affecting the left ventricle were recently discovered.
Hajar El Ouartassi, MD, Raid Faraj, MD, Zakariae Laraichi, MD, Rhita Ezzahraoui, MD, Zaineb Bourouhou, MD, Nawal Doghmi, PhD, Mohamed Cherti, PhD   +6 more
doaj   +1 more source

Late presentation of arrhythmogenic right ventricular cardiomyopathy: a case report

Journal of Medical Case Reports, 2009
Introduction Arrhythmogenic right ventricular cardiomyopathy is an inherited myocardial disease affecting predominantly young people and manifests as sustained ventricular tachycardia with left bundle branch block morphology, sudden death or isolated ...
Papaioannou Georgios I, Apostolopoulos Theodoros, Stambola Sotiria, Zilidis Antonios, Gialafos John   +4 more
doaj   +1 more source