Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern

BACKGROUND: Limb girdle muscular dystrophy type 2G (LGMD2G) is a subtype of autosomal recessive muscular dystrophy caused by mutations in the telethonin gene. There are few LGMD2G patients worldwide reported, and this is the first description associated with early tibialis anterior sparing on muscle...

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Detalles Bibliográficos
Autores principales: Cotta, Ana, Paim, Julia Filardi, da-Cunha-Junior, Antonio Lopes, Neto, Rafael Xavier, Nunes, Simone Vilela, Navarro, Monica Magalhaes, Valicek, Jaquelin, Carvalho, Elmano, Yamamoto, Lydia U, Almeida, Camila F, Braz, Shelida Vasconcelos, Takata, Reinaldo Issao, Vainzof, Mariz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4188961/
https://www.ncbi.nlm.nih.gov/pubmed/25298746
http://dx.doi.org/10.1186/1472-6890-14-41

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4188961/
https://www.ncbi.nlm.nih.gov/pubmed/25298746
http://dx.doi.org/10.1186/1472-6890-14-41

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