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Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality

Abstract Background Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is associated with ventricular arrhythmia, heart failure (HF), and sudden death. Thromboembolism is also an important and serious complication of ARVC/D. However, the etiology of ARVC/D and thromboembolism and the...

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Autori principali: Jia Chen, Yuting Ma, Hong Li, Zhuo Lin, Zhe Yang, Qin Zhang, Feng Wang, Yanping Lin, Zebing Ye, Yubi Lin
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMC 2022-05-01
Serie:Orphanet Journal of Rare Diseases
Soggetti:
Cardiomyopathy
Arrhythmogenic right ventricular cardiomyopathy/dysplasia
Sudden death
Arrhythmia
Thromboembolism
Gene
Accesso online:https://doi.org/10.1186/s13023-022-02348-z
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