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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Dettagli Bibliografici
Pubblicato in:eNeurologicalSci
Autori principali: Morimoto, Nobutoshi, Morimoto, Mizuki, Takahashi, Yoshiaki, Takamiya, Motonori, Nishino, Ichizo, Abe, Koji
Natura: Artigo
Lingua:Inglês
Pubblicazione: Elsevier 2020
Soggetti:
Case Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7642826/
https://ncbi.nlm.nih.gov/pubmed/33195829
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ensci.2020.100284
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