Myofibrillar Cardiomyopathy due to a Novel Desmin Gene Mutation: Complementary Role of Echocardiography, Cardiac Magnetic Resonance, and Genetic Testing in Delineating Diagnosis

The investigators present a rare case of myofibrillar cardiomyopathy in an 18-year-old male patient in which echocardiography, cardiac magnetic resonance, and genetic testing played complementary roles. At the top, the parasternal long- and short-axis views of the heart document increased wall thick...

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Detalles Bibliográficos
Autores principales: Koitka, Karen, Dahiya, Arun, Lo, Ada, Scalia, Gregory M., Atherton, John J., Prasad, Sandhir B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Cardiomyopathy
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034477/
https://www.ncbi.nlm.nih.gov/pubmed/30062237
http://dx.doi.org/10.1016/j.case.2016.11.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034477/
https://www.ncbi.nlm.nih.gov/pubmed/30062237
http://dx.doi.org/10.1016/j.case.2016.11.001

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