Results 111 to 120 of about 26,419 (210)

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

Heart MRI Images Analysis in Case of Arrythmogenic Right Ventricular Cardiomyopathy (ARVC) [PDF]

, 2018
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is a cause of sudden cardiac death in otherwise healthy young adults. (ARVD/C) is an inherited cardiomyopathy characterized by life-threatening ventricular arrhythmias and slowly progressive ...
Apriantoro, N. H. (Nursama), Sari, G. (Gando), Sriyatun, S. (Sriyatun)   +2 more
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Genotype-phenotype correlations in patients with pathogenic/likely pathogenic titin variants from the Swiss Arrhythmogenic Cardiomyopathy Registry

Open Heart
Background Truncating variants in the titin gene (TTNtv) are associated with cardiomyopathy, mainly dilated cardiomyopathy (DCM). The clinical presentation and outcomes of arrhythmogenic phenotypes in these patients are scarcely studied.Methods and ...
Andreas J Flammer, Lorraine Sazgary, Robert Manka, Annina Salome Vischer, Ardan M Saguner, Frank Ruschitzka, Marina Rieder, Siv Fokstuen, Firat Duru, Umberto Maccio, Argelia Medeiros-Domingo, Corinna Brunckhorst, Felix Tanner, Verena Charlotte Wilzeck, Nina Alissa Schätti, Matthias P. Nägele, Fran Mikulicic, Christian Grebmer, Katja E Odening, Nicole R Bonetti   +19 more
doaj   +1 more source

Mouse models in Arrhythmogenic Right Ventricular Cardiomyopathy

Frontiers in Physiology, 2012
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disorder characterized by fibrofatty replacement of cardiomyocytes. The cardinal manifestations are arrhythmias, sudden cardiac death and seldom heart failure.
Elisabeth M Lodder, Stefania eRizzo
doaj   +1 more source

Carvajal syndrome: a brief overview and clinical case of cardiomyopathy, associated with compound heterozygous mutations of the desmoplakin gene

Российский кардиологический журнал, 2018
Mutations in the genes encoding desmosomal proteins cause a wide range of diseases associated with abnormalities of the skin, hair and heart. In 45-50% these mutations determine the development of arrhythmogenic right ventricular cardiomyopathy.
T. G. Vaikhanskaya, L. N. Sivitskaya, T. V. Kurushko, D. P. Ermakovich, E. V. Zasim, N. G. Danilenko   +5 more
doaj   +1 more source

Case Report: Contrasting phenotypes of arrhythmogenic cardiomyopathy: classic desmosomal ARVC and a RIT1-related phenocopy

Frontiers in Cardiovascular Medicine
BackgroundArrhythmogenic right ventricular cardiomyopathy (ARVC) is most commonly associated with pathogenic variants in desmosomal genes. However, ARVC-like phenotypes may also arise from non-desmosomal genetic backgrounds, creating diagnostic ...
Bo Eun Park, Bo Eun Park, Dong Heon Yang, Dong Heon Yang   +3 more
doaj   +1 more source

Sudden Cardiac Death in Athletes: Magnitude, Causes, and Prevention Strategies - A Literature Review

Quality in Sport
Sudden cardiac death (SCD) in athletes, though rare, is the leading cause of exercise-related mortality and poses significant concern due to the symbolic health and vitality of athletes.
Bohdan Melnyk, Artur Rygielski, Emilia Latour, Marianna Latour, Roksana Judek, Mariia Melnyk   +5 more
doaj   +1 more source

ATIPICIDADES EN UN CASO CON DISPLASIA ARRITMOGÉNICA DEL VENTRÍCULO DERECHO O ENFERMEDAD DE UHL / Report of an atypical case with arrhythmogenic right ventricular dysplasia or Uhl´s anomaly [PDF]

, 2012
ResumenLa displasia arritmogénica del ventrículo derecho es una miocardiopatía caracterizada por arritmias ventriculares malignas y anomalías estructurales progresivas, que afectan primariamente al ventrículo derecho.
Ana M. Jerez Castro, Aníbal González Trujillo, Eliezer San Román García, Luis M. Morales Pérez, Omar R. González Greck   +4 more
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Arrhythmogenic Right Ventricular Cardiomyopathy Diagnosed with 2020 International Criteria

Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare cardiomyopathy. Early diagnosis is important to prevent mortality. They have a high risk of sudden cardiac death due to ventricular arrhythmia, which requires the implantation of a ...
Neelesh Damor, Nitin Modi, Atul Karande, Ashish Mishra, Sunil Sharma   +4 more
doaj   +1 more source

Epicardial myocardial strain abnormalities may identify the earliest stages of arrhythmogenic cardiomyopathy. [PDF]

, 2016
The aim of this cohort study was to evaluate the value of echocardiographic multilayer strain analysis in the identification of arrhythmogenic cardiomyopathy (AC) in its earliest stages in which sudden cardiac death can occurs.
Castelletti, S, Cheang, MH, Hauer, AD, Lafitte, S, McKenna, WJ, Moon, JC, Pantazis, A, Peyrou, J, Rosmini, S, Réant, P, Syrris, P, Tomé-Esteban, M   +11 more
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