Arrhythmogenic cardiomyopathy

D Corrado, C Basso, DP Judge - Circulation research, 2017 - Am Heart Assoc
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to
sudden cardiac death, particularly in young patients and athletes. Pathological features …

Clinical Diagnosis, Imaging, and Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: JACC State-of-the-Art Review

E Gandjbakhch, A Redheuil, F Pousset… - Journal of the American …, 2018 - jacc.org
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited
cardiomyopathy that can lead to sudden cardiac death and heart failure. Our understanding …

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy

JA Towbin, WJ McKenna, DJ Abrams, MJ Ackerman… - Heart rhythm, 2019 - Elsevier
Arrhythmogenic cardiomyopathy (ACM) is an arrhythmogenic disorder of the myocardium
not secondary to ischemic, hypertensive, or valvular heart disease. ACM incorporates a …

International evidence based reappraisal of genes associated with arrhythmogenic right ventricular cardiomyopathy using the clinical genome resource framework

CA James, JDH Jongbloed… - Circulation: Genomic …, 2021 - Am Heart Assoc
Background: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited
disease characterized by ventricular arrhythmias and progressive ventricular dysfunction …

Molecular mechanisms of arrhythmogenic cardiomyopathy

KM Austin, MA Trembley, SF Chandler… - Nature Reviews …, 2019 - nature.com
Arrhythmogenic cardiomyopathy is a genetic disorder characterized by the risk of life-
threatening arrhythmias, myocardial dysfunction and fibrofatty replacement of myocardial …

An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis

D Chatterjee, M Fatah, D Akdis, DA Spears… - European heart …, 2018 - academic.oup.com
Aims Arrhythmogenic right ventricular cardiomyopathy (ARVC) is characterized by right
ventricular myocardial replacement and life-threatening ventricular arrhythmias …

Diagnostic and therapeutic strategies for arrhythmogenic right ventricular dysplasia/cardiomyopathy patient

W Wang, CA James, H Calkins - Ep Europace, 2019 - academic.oup.com
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a rare inherited
heart muscle disease characterized by ventricular tachyarrhythmia, predominant right …

Desmosomal protein degradation as an underlying cause of arrhythmogenic cardiomyopathy

H Tsui, SJ van Kampen, SJ Han, V Meraviglia… - Science translational …, 2023 - science.org
Arrhythmogenic cardiomyopathy (ACM) is an inherited progressive cardiac disease. Many
patients with ACM harbor mutations in desmosomal genes, predominantly in plakophilin-2 …

Definition and treatment of arrhythmogenic cardiomyopathy: an updated expert panel report

PM Elliott, A Anastasakis, A Asimaki… - European journal of …, 2019 - Wiley Online Library
It is 35 years since the first description of arrhythmogenic right ventricular cardiomyopathy
(ARVC) and more than 20 years since the first reports establishing desmosomal gene …

Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis

ET Hoorntje, WP Te Rijdt, CA James… - Cardiovascular …, 2017 - academic.oup.com
Arrhythmogenic cardiomyopathy (ACM) is a rare, heritable heart disease characterized by
fibro-fatty replacement of the myocardium and a high degree of electric instability. It was first …