A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis

Facioscapulohumeral muscular dystrophy (FSHD) is a common inherited muscular dystrophy presented clinically with slowly progressive weakness and wasting of facial and limb muscles and rare bulbar muscle involvement. We present herein a 70-year-old man who was a known case of FSHD with complaint of 1...

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Detalles Bibliográficos
Autores principales: Asadollahi, Marjan, Rezaiyan, Bibiseyedeh, Amjadi, Hiva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829232/
https://www.ncbi.nlm.nih.gov/pubmed/24250856

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829232/
https://www.ncbi.nlm.nih.gov/pubmed/24250856

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