The role of genetic testing in suspected fulminant myocarditis: A case report

ACM is a rare hereditary heart disease characterized by a progressive fibro-fatty replacement of the myocardium that can affect either the right or the left ventricle or both. It is mainly caused by variants in the desmosome genes with autosomal dominant transmission and incomplete penetrance. The d...

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Detalles Bibliográficos
Autores principales: Mistrulli, Raffaella, Micolonghi, Caterina, Follesa, Federico, Fabiani, Marco, Pagannone, Erika, D'Amati, Giulia, Giordano, Carla, Caroselli, Silvia, Savio, Camilla, Germani, Aldo, Pizzuti, Antonio, Visco, Vincenzo, Petrucci, Simona, Rubattu, Speranza, Piane, Maria, Autore, Camillo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470308/
https://www.ncbi.nlm.nih.gov/pubmed/37662494
http://dx.doi.org/10.1016/j.ymgmr.2023.101000

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470308/
https://www.ncbi.nlm.nih.gov/pubmed/37662494
http://dx.doi.org/10.1016/j.ymgmr.2023.101000

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