Results 21 to 30 of about 979 (102)

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

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

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

Familial Recurrent Myocarditis Triggered by Exercise in Patients With a Truncating Variant of the Desmoplakin Gene

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2020
Background Variants of the desmosomal protein desmoplakin are associated with arrhythmogenic cardiomyopathy, an important cause of ventricular arrhythmias in children and young adults.
Wolfgang Poller, Jan Haas, Karin Klingel, Jirko Kühnisch, Martina Gast, Ziya Kaya, Felicitas Escher, Elham Kayvanpour, Franziska Degener, Bernd Opgen‐Rhein, Felix Berger, Hans‐Christian Mochmann, Carsten Skurk, Bettina Heidecker, Heinz‐Peter Schultheiss, Lorenzo Monserrat, Benjamin Meder, Ulf Landmesser, Sabine Klaassen   +18 more
doaj   +1 more source

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

Arrhythmogenic Ventricular Cardiomyopathy

JACC: Case Reports, 2021
After a 20-year-old woman suddenly died, autopsy showed characteristic findings of biventricular arrhythmogenic cardiomyopathy. Screening of her family members revealed the same desmoplakin gene mutation and imaging abnormalities predominantly involving ...
Aranyak S. Rawal, MD, Tara VanCleave, BS, Neeraja Yedlapati, MD, Jeffery E. Saffitz, MD, PhD, William James Craigen, MD, PhD, John L. Jefferies, MD, MPH   +5 more
doaj   +1 more source

Arrhythmogenic left ventricular cardiomyopathy [PDF]

Heart, 2021
### Learning objectives Arrhythmogenic cardiomyopathy (ACM) is a genetic heart muscle disease characterised by substitution of the ventricular myocardium by fibrofatty tissue.1 The disease was originally termed ‘arrhythmogenic right ventricular (dysplasia/) cardiomyopathy’ (ARVC) to define a condition which distinctively affected the right ventricle ...
Corrado D., Basso C.
openaire   +3 more sources

Arrhythmogenic cardiomyopathy in a cat [PDF]

Ciência Rural
: Arrhythmogenic cardiomyopathy is a rare cardiac disease in cats, characterized by ventricular myocyte atrophy and replacement by fibrofatty tissue, predisposing to potentially fatal arrhythmias and heart failure.
André Rodrigues Carvalho Netto, Lorrayne dos Santos Miranda, Juarez Henrique Ferreira, Laura Monteiro de Castro Conti, Daniela Campagnol, Cristiane dos Santos Honsho, Talita Mariana Morata Raposo-Ferreira   +6 more
doaj   +2 more sources

Catheter Ablation in Arrhythmic Cardiac Diseases: Endocardial and Epicardial Ablation

Reviews in Cardiovascular Medicine, 2022
Arrhythmogenic cardiomyopathy (ACM) is a group of arrhythmogenic disorders of the myocardium that are not caused by ischemic, hypertensive, or valvular heart disease.
Wen-Han Cheng, Fa-Po Chung, Yenn-Jiang Lin, Li-Wei Lo, Shih-Lin Chang, Yu-Feng Hu, Ta-Chuan Tuan, Tze-Fan Chao, Jo-Nan Liao, Chin-Yu Lin, Ting-Yung Chang, Ling Kuo, Cheng-I Wu, Chih-Min Liu, Shin-Huei Liu, Shih-Ann Chen   +15 more
doaj   +1 more source

Arrhythmogenic potential of cardiomyopathies

Медицина неотложных состояний
The article presents a review of literary scientific sources from the MEDLINE database on PubMed, Web of Science, Scopus, and Google Scholar platforms, focusing on arrhythmia in patients with arrhythmogenic cardiomyopathy.
O.M. Kovalova, V.V. Nikonov, A.K. Zhuravlova, V.V. Nikonova, Ye.I. Kinoshenko, M.P. Baturynskyi   +5 more
doaj   +1 more source