Mixed Hypertrophic and Dilated Phenotype of Cardiomyopathy in a Patient With Homozygous In-Frame Deletion in the MyBPC3 Gene Treated as Myocarditis for a Long Time

Hypertrophic cardiomyopathy (HCM) is the most common inherited disease, with a prevalence of 1:200 worldwide. The cause of HCM usually presents with an autosomal dominant mutation in the genes encoding one of more than 20 sarcomeric proteins, incomplete penetrance, and variable expressivity. HCM cla...

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Detalles Bibliográficos
Autores principales: Blagova, Olga, Alieva, Indira, Kogan, Eugenia, Zaytsev, Alexander, Sedov, Vsevolod, Chernyavskiy, S., Surikova, Yulia, Kotov, Ilya, Zaklyazminskaya, Elena V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546790/
https://www.ncbi.nlm.nih.gov/pubmed/33101033
http://dx.doi.org/10.3389/fphar.2020.579450

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546790/
https://www.ncbi.nlm.nih.gov/pubmed/33101033
http://dx.doi.org/10.3389/fphar.2020.579450

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