A case of type 1 facioscapulohumeral muscular dystrophy (FSHD) with restrictive ventilatory defect and congestive heart failure

[Background] Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant muscle disease characterized by asymmetric involvement of muscles in the face, upper extremity, trunk, and lower extremity regions, with variable severity. It was recently reported that restrictive respiratory involv...

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Detalles Bibliográficos
Autores principales: Morimoto, Nobutoshi, Morimoto, Mizuki, Takahashi, Yoshiaki, Takamiya, Motonori, Nishino, Ichizo, Abe, Koji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642826/
https://www.ncbi.nlm.nih.gov/pubmed/33195829
http://dx.doi.org/10.1016/j.ensci.2020.100284

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642826/
https://www.ncbi.nlm.nih.gov/pubmed/33195829
http://dx.doi.org/10.1016/j.ensci.2020.100284

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