Early detection of cardiac involvement in Miyoshi myopathy: 2D strain echocardiography and late gadolinium enhancement cardiovascular magnetic resonance

BACKGROUND: Miyoshi myopathy (MM) is an autosomal recessive distal myopathy characterized by early adult onset. Cardiomyopathy is a major clinical manifestation in other muscular dystrophies and an important prognostic factor. Although dysferlin is highly expressed in cardiac muscle, the effect of d...

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Detalles Bibliográficos
Autores principales: Choi, E Ryoung, Park, Sung-Ji, Choe, Yeon Hyeon, Ryu, Dong Ryeol, Chang, Sung-A, Choi, Jin-Oh, Lee, Sang-Chol, Park, Seung Woo, Kim, Byoung Joon, Kim, Duk-Kyung, Oh, Jae K
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887439/
https://www.ncbi.nlm.nih.gov/pubmed/20497525
http://dx.doi.org/10.1186/1532-429X-12-31

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887439/
https://www.ncbi.nlm.nih.gov/pubmed/20497525
http://dx.doi.org/10.1186/1532-429X-12-31

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