Results 11 to 20 of about 14,748 (188)

Multimodality imaging in arrhythmogenic cardiomyopathy [PDF]

Romanian Journal of Cardiology, 2021
Arrhythmogenic cardiomyopathy, as it has been recently redefined, is characterized by progressive myocyte loss with fibrosis and fat infiltration of the myocardium, which finally leads to a broad clinical spectrum ranging from heart failure symptoms to ...
Laura Tapoi, Alexandra Clement, Rodica Radu, Radu Sascau   +3 more
doaj   +1 more source

Novel Risk Prediction Model to Determine Adverse Heart Failure Outcomes in Arrhythmogenic Right Ventricular Cardiomyopathy

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2022
Background Patients with arrhythmogenic right ventricular cardiomyopathy are at risk for life‐threatening ventricular tachyarrhythmias, but progressive heart failure (HF) may occur in later stages of disease.
Shi Chen, Liang Chen, Ardan M. Saguner, Kai Chen, Deniz Akdis, Alessio Gasperetti, Corinna Brunckhorst, Hanwei Tang, Guangran Guo, Man Rao, Xiangjie Li, Jiangping Song, Firat Duru, Shengshou Hu   +13 more
doaj   +1 more source

Prominent Epsilon Waves in a Patient With Cardiac Sarcoidosis

JACC: Case Reports, 2020
Epsilon waves are the surface manifestation of myocardial regions with delayed activation and are considered the hallmark of arrhythmogenic right ventricular cardiomyopathy.
Kevin J. Mills, MD, Mauricio Sendra Ferrer, MD, Mario D. Gonzalez, MD   +2 more
doaj   +1 more source

Arrhythmogenic Cardiomyopathy—Further Insight into the Clinical Spectrum of Desmoplakin Disease

Cardiogenetics, 2021
Arrhythmogenic cardiomyopathy is a familial heart muscle disease characterized by structural, electrical, and pathological abnormalities. Recognition of left ventricular (LV) involvement in arrhythmogenic right ventricular cardiomyopathy (ARVC) has led ...
Joanne Simpson, Joan Anusas, Denise Oxnard, Sylvia Wright, Ruth McGowan, Caroline Coats   +5 more
doaj   +1 more source

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

Establishment of a Dedicated Inherited Cardiomyopathy Clinic: From Challenges to Improved Patients’ Outcome

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2022
Background Inherited cardiomyopathies (ICs) are relatively rare. General cardiologists have little experience in diagnosing and managing these conditions. International societies have recognized the need for dedicated IC clinics.
Emily Smith, Paul D. Thompson, Carolyn Burke‐Martindale, Adaya Weissler‐Snir   +3 more
doaj   +1 more source

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

Right Ventricular Fatty Infiltration With an Abnormal ECG

JACC: Case Reports, 2021
Two middle-aged women had evidence suggesting right ventricular hypertrophy on routine electrocardiograms. Their echocardiograms showed right ventricular thickening and cardiac magnetic resonance imaging revealed right ventricular fatty infiltration ...
Natalija Odanovic, MD, Hamid R. Mojibian, MD, Lawrence H. Young, MD   +2 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

A case of arrhythmogenic right ventricular cardiomyopathy [PDF]

Canadian Journal of Cardiology, 2008
The present report describes a 40-year-old woman with a long history of monomorphic ventricular tachycardia and left bundle branch block. She was treated with various antiarrhythmic agents; ventricular tachycardia ablation was attempted and an automatic implantable cardioverter defibrillator was implanted.
Sorel, Goland, Lawrence S C, Czer, Daniel, Luthringer, Robert J, Siegel   +3 more
openaire   +2 more sources