Autosomal Dominant Centronuclear Myopathy with Unique Clinical Presentations

Centronuclear myopathies are clinically and genetically heterogenous diseases with common histological findings, namely, centrally located nuclei in muscle fibers with a predominance and hypotrophy of type 1 fibers. We describe two cases from one family with autosomal dominant centronuclear myopathy...

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Detalles Bibliográficos
Autores principales: Lee, Jee-Young, Min, Ju-Hong, Hong, Yoon-Ho, Sung, Jung-Joon, Park, Sung-Hye, Park, Seong-Ho, Lee, Kwang-Woo, Park, Kyung Seok
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2007
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694645/
https://www.ncbi.nlm.nih.gov/pubmed/18162732
http://dx.doi.org/10.3346/jkms.2007.22.6.1098

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694645/
https://www.ncbi.nlm.nih.gov/pubmed/18162732
http://dx.doi.org/10.3346/jkms.2007.22.6.1098

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