Results 51 to 60 of about 979 (102)

Treatment of arrhythmogenic right ventricular cardiomyopathy (dysplasia) [PDF]

Кардіохірургія та інтервенційна кардіологія, 2016
Arrhythmogenic right ventricular cardiomyopathy (dysplasia) is an inheritable heart muscle disease predisposing to ventricular arrhythmias and increasing risk of sudden cardiac death.
M.Т. Vatutin, G.S. Smyrnova, Y.V. Yeshchenko, G.E. Degtiarova, V.S. Kolesnikov, Y.P. Gritsenko   +5 more
doaj  

Relationship Between Electrocardiographic Findings and Cardiac Magnetic Resonance Phenotypes in Arrhythmogenic Cardiomyopathy

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2018
Background The new designation of arrhythmogenic cardiomyopathy defines a broader spectrum of disease phenotypes, which include right dominant, biventricular, and left dominant variants. We evaluated the relationship between electrocardiographic findings
Manuel De Lazzari, Alessandro Zorzi, Alberto Cipriani, Angela Susana, Giulio Mastella, Alessandro Rizzo, Ilaria Rigato, Barbara Bauce, Benedetta Giorgi, Carmelo Lacognata, Sabino Iliceto, Domenico Corrado, Martina Perazzolo Marra   +12 more
doaj   +1 more source

Recurrent Syncope in a Young Man: What Lies Underneath?

Indian Journal of Clinical Cardiology
Arrhythmogenic right ventricular cardiomyopathy is an autosomal dominant genetic disease which leads to fatty replacement of the right ventricular myocardium, leading to the occurrence of ventricular arrhythmia.
Deepanjan Bhattacharya, Koyel Chakraborty, Ajay Gautam, Basudeb Bhattacharjee   +3 more
doaj   +1 more source

Sudden cardiac death in patients with nonischemic cardiomyopathy

Indian Heart Journal, 2014
Sudden cardiac death (SCD) is an important cause of mortality worldwide. Although SCD is most often associated with coronary heart disease, the risk of SCD in patients without ischemic heart disease is well-established.
Brian P. Betensky, Sanjay Dixit
doaj   +1 more source

Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy.

PLoS ONE, 2015
Mutations in the lamin A/C gene (LMNA) were associated with dilated cardiomyopathy (DCM) and, recently, were related to severe forms of arrhythmogenic right ventricular cardiomyopathy (ARVC).
Cinzia Forleo, Monica Carmosino, Nicoletta Resta, Alessandra Rampazzo, Rosanna Valecce, Sandro Sorrentino, Massimo Iacoviello, Francesco Pisani, Giuseppe Procino, Andrea Gerbino, Arnaldo Scardapane, Cristiano Simone, Martina Calore, Silvia Torretta, Maria Svelto, Stefano Favale   +15 more
doaj   +1 more source

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

Right ventricular assessment of the adolescent footballer’s heart

Echo Research and Practice
Introduction Athletic training can result in electrical and structural changes of the right ventricle that may mimic phenotypical features of arrhythmogenic right ventricular cardiomyopathy (ARVC), such as T-wave inversion and right heart dilatation.
D. X. Augustine, J. Willis, S. Sivalokanathan, C. Wild, A. Sharma, A. Zaidi, K. Pearce, G. Stuart, M. Papadakis, S. Sharma, A. Malhotra   +10 more
doaj   +1 more source

LV‐predominant arrhythmogenic cardiomyopathy related to pathogenic DSP‐variant

Clinical Case Reports
Key Clinical Message In contrast to previously thought, arrhythmogenic cardiomyopathy can occur exclusively in the left ventricle in association with autosomal dominant mutation, even without any skin manifestations.
Soban Ahmad, Husam El Sharu, Robin Fernandes, Mark Kolasa, Constantin Bogdan Marcu   +4 more
doaj   +1 more source

Catheter Ablation of Ventricular Tachycardia in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: A Sequential Approach

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2019
Background It has been suggested that endocardial and epicardial ablation of ventricular tachycardia (VT) improves outcome in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Shibu Mathew, Ardan M. Saguner, Niklas Schenker, Lukas Kaiser, Pengpai Zhang, Yoshiga Yashuiro, Christine Lemes, Thomas Fink, Tilman Maurer, Francesco Santoro, Peter Wohlmuth, Bruno Reißmann, Christian H. Heeger, Roland Tilz, Erik Wissner, Andreas Rillig, Andreas Metzner, Karl‐Heinz Kuck, Feifan Ouyang   +18 more
doaj   +1 more source

Rapid progression of right ventricular dysfunction: a case report

BMC Cardiovascular Disorders
Background Arrhythmogenic cardiomyopathy (ACM) is a genetic myocardial disease characterized by progressive myocyte loss and fibrofatty (fibrous and adipose) tissue replacement to predispose these patients to fatal ventricular arrhythmias and impairment ...
Guoliang Li, Changying Zhao, Lingmin Wu, Yang Yan   +3 more
doaj   +1 more source