Characterisation of patients referred to a tertiary-level inherited cardiac condition clinic with suspected arrhythmogenic right ventricular cardiomyopathy (ARVC)

Abstract Background Arrhythmogenic right ventricular cardiomyopathy (ARVC) or arrhythmogenic cardiomyopathy is a rare inherited disease with incomplete penetrance and an environmental component. Although a rare disease, ARVC is a common cause of sudden cardiac death in young adults. Data on the diff...

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Autors principals:	A. Aljehani, T. Kew, S. Baig, H. Cox, L. C. Sommerfeld, B. Ensam, M. Kalla, R. P. Steeds, L. Fabritz
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2023-01-01
Col·lecció:	BMC Cardiovascular Disorders
Matèries:	Arrhythmogenic right ventricular cardiomyopathy Arrhythmogenic cardiomyopathy Electrocardiography Cardiac magnetic resonance imaging Echocardiography
Accés en línia:	https://doi.org/10.1186/s12872-022-03021-w
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