Results 11 to 20 of about 105,745 (208)

Biventricular Arrhythmogenic Cardiomyopathy Mimicking Cardiac Sarcoidosis

JACC: Case Reports
Noninvasive imaging is crucial for diagnosing and managing arrhythmogenic cardiomyopathy. Despite advanced multimodality imaging tools, challenges persist in differentiating it from other arrhythmogenic diseases (eg, cardiac sarcoidosis).
Mouna Kodali, MD, Patrycja Galazka, MD, Asad Ghafoor, Atul Bhatia, Suhail Q. Allaqaband, MD   +4 more
doaj   +2 more sources

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   +1 more source

Inflammation—A Possible Link between Myocarditis and Arrhythmogenic Cardiomyopathy

Diagnostics
Arrhythmogenic cardiomyopathy is a primary genetic disease caused by mutations in the desmosome genes. Ever since the introduction of new imaging techniques, like cardiovascular magnetic resonance, the diagnosis of arrhythmogenic cardiomyopathy has ...
Ioan Radu Lala, Adina Pop-Moldovan
doaj   +2 more sources

Late presentation of arrhythmogenic right ventricular cardiomyopathy: a case report [PDF]

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   +2 more sources

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

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

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

Molecular genetics of arrhythmogenic right ventricular cardiomyopathy in South Africa [PDF]

, 2011
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heritable disorder characterised by progressive degeneration of the right ventricular myocardium, arrhythmias and an increased risk of sudden death at a young age. Fourteen chromosomal loci have
Blanckenberg, Janine
core   +1 more source