Case Report: Identification of novel CDH2 mutation (p. P183A het)-induced arrhythmogenic cardiomyopathy in China

Case Report: Identification of novel CDH2 mutation (p. P183A het)-induced arrhythmogenic cardiomyopathy in China

BackgroundArrhythmogenic cardiomyopathy/dysplasia (ACM) is an inheritable heart disease closely related to gene variations induced heart fibrofatty replacement, which increases the risk of arrhythmia events and even sudden cardiac death. In this study, we reported a 10-year-old patient with a novel...

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Bibliographic Details
Main Authors: Kun Li, Yifei Wang, Jing Yang, Fang Liu, Fulan Liu, Ping Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-11-01
Series:Frontiers in Cardiovascular Medicine
Subjects:
ACM
CDH2
cadherin-2
mutation
adolescence
Online Access:https://www.frontiersin.org/articles/10.3389/fcvm.2023.1258807/full

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