作者: Mingchang Zhang , Fabio Tavora , Ling Li , David Fowler , Ziqin Zhao
DOI: 10.1097/PAT.0B013E32835A0163
关键词:
摘要: Summary Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an uncommon heart disease characterised by arrhythmias, scarring, and fibrofatty change. Although mutations in the desmosome have been frequently observed patients clinically diagnosed with ARVC, recent data put a direct causal relationship question. Many ARVC not had histological confirmation, many family members are affected. Desmosomal found other cardiac diseases, specificity of histopathological features even We aim to review purported link between critical analysis reported data.