Misdiagnosed myocarditis in arrhythmogenic cardiomyopathy induced by a homozygous variant of DSG2: a case report

BACKGROUND: Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiomyopathy that is rarely diagnosed in infants or young children. However, some significant homozygous or compound heterozygous variants contribute to more severe clinical manifestations. In addition, inflammation of the myocardium...

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Detalles Bibliográficos
Autores principales: Liu, Xuwei, Zhang, Yue, Li, Wenjuan, Zhang, Qian, Zhou, Letao, Hua, Yimin, Duan, Hongyu, Li, Yifei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242036/
https://www.ncbi.nlm.nih.gov/pubmed/37288269
http://dx.doi.org/10.3389/fcvm.2023.1150657

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242036/
https://www.ncbi.nlm.nih.gov/pubmed/37288269
http://dx.doi.org/10.3389/fcvm.2023.1150657

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