Echocardiographic diagnosis of the different phenotypes of hypertrophic cardiomyopathy

Hypertrophic Cardiomyopathy (HCM) is an inherited cardiovascular disorder of great genetic heterogeneity and has a prevalence of 0.1 – 0.2 % in the general population. Several hundred mutations in more than 27 genes, most of which encode sarcomeric structures, are associated with the HCM phenotype....

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Detalles Bibliográficos
Autores principales: Parato, Vito Maurizio, Antoncecchi, Valeria, Sozzi, Fabiola, Marazia, Stefania, Zito, Annapaola, Maiello, Maria, Palmiero, Pasquale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982201/
https://www.ncbi.nlm.nih.gov/pubmed/27519172
http://dx.doi.org/10.1186/s12947-016-0072-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982201/
https://www.ncbi.nlm.nih.gov/pubmed/27519172
http://dx.doi.org/10.1186/s12947-016-0072-5

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