Case report: Mutation in NPPA gene as a cause of fibrotic atrial myopathy

Early-onset atrial fibrillation (AF) can be the manifestation of a genetic atrial myopathy. However, specific genetic identification of a mutation causing atrial fibrosis is rare. We report a case of a young patient with an asymptomatic AF, diagnosed during a routine examination. The cardiac MRI rev...

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Detalles Bibliográficos
Autores principales: Silva Cunha, Pedro, Antunes, Diana Oliveira, Laranjo, Sérgio, Coutinho, Ana, Abecasis, João, Oliveira, Mário Martins
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/PMC10285104/
https://www.ncbi.nlm.nih.gov/pubmed/37363091
http://dx.doi.org/10.3389/fcvm.2023.1149717

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285104/
https://www.ncbi.nlm.nih.gov/pubmed/37363091
http://dx.doi.org/10.3389/fcvm.2023.1149717

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