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

BMC Cardiovascular Disorders

Research

B. Ensam¹  M. Kalla²  S. Baig²  T. Kew²  R. P. Steeds²  L. Fabritz³  A. Aljehani⁴  L. C. Sommerfeld⁵  H. Cox⁶ 

[1] Department of Cardiology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK;Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK;Department of Cardiology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK;Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK;Department of Cardiology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK;Department of Cardiology, University Heart and Vascular Centre Hamburg, UKE Hamburg and DZHK, Hamburg/Kiel/Luebeck, Germany;University Centre of Cardiovascular Science, UKE Hamburg, Hamburg, Germany;Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK;Department of Cardiology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK;King Saud Bin Abdulaziz University For Health Sciences, Echocardiography Cardiovascular Technology (ECVT) Program, Riyadh, Saudi Arabia;Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK;University Centre of Cardiovascular Science, UKE Hamburg, Hamburg, Germany;West Midlands Regional Genetics Unit, Clinical Genetics, Birmingham Women’s and Children’s NHS Foundation Trust (BWC) Birmingham, Birmingham, UK;

关键词: Arrhythmogenic right ventricular cardiomyopathy;    Arrhythmogenic cardiomyopathy;    Electrocardiography;    Cardiac magnetic resonance imaging;    Echocardiography;   

DOI  :  10.1186/s12872-022-03021-w

 received in 2022-06-28, accepted in 2022-12-19,  发布年份 2022

来源: Springer

【 授权许可】

CC BY   
© The Author(s) 2023

【 图 表 】

Fig. 1 

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