Arrhythmogenic Cardiomyopathy: A Review of a Rare Case of Biventricular Phenotype

Arrhythmogenic cardiomyopathy is a rare hereditary structural heart disease, with various phenotypes, which mostly affects the right ventricle of the heart, resulting in fibrofatty replacement of the heart muscles and a proclivity to create spontaneous malignant cardiac arrhythmias that may lead to...

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Detalles Bibliográficos
Autores principales: Aiwuyo, Henry O, Javed, Gulfam, Ataiyero, Omotomilola, Ibeson, Emeka C, Torere, Beatrice, Umuerri, Ejiro M, El Hadj Othmane, Taha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Cardiac/Thoracic/Vascular Surgery
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637405/
https://www.ncbi.nlm.nih.gov/pubmed/36381856
http://dx.doi.org/10.7759/cureus.30040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637405/
https://www.ncbi.nlm.nih.gov/pubmed/36381856
http://dx.doi.org/10.7759/cureus.30040

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