Severe hypertrophic cardiomyopathy in a patient with a homozygous MYH7 gene variant

BACKGROUND: Hypertrophic cardiomyopathy is an autosomal dominant disease. The main feature of this disorder is its occurrence in patients who present a left ventricular hypertrophy, unexplained by the loading conditions, usually asymmetric with greatest involvement most commonly of the interventricu...

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Detalles Bibliográficos
Autores principales: Serra, Walter, Vitetta, Giulia, Uliana, Vera, Barocelli, Federico, Barili, Valeria, Allegri, Isabella, Ardissino, Diego, Gualandi, Francesca, Percesepe, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803765/
https://www.ncbi.nlm.nih.gov/pubmed/36593836
http://dx.doi.org/10.1016/j.heliyon.2022.e12373

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803765/
https://www.ncbi.nlm.nih.gov/pubmed/36593836
http://dx.doi.org/10.1016/j.heliyon.2022.e12373

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