Facioscapulohumeral muscular dystrophy (FSHD) and multiple sclerosis: a case report

Facioscapulohumeral muscular dystrophy 1 (FSHD1) is an autosomal dominant neuromuscular disorder, associated with reduction of tandemly arrayed repetitive DNA elements D4Z4 (DRA), at 4q35. Few cases, especially carriers of 1-3 DRA show a syndromic form. Anecdotally the association of FSHD with multi...

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Detalles Bibliográficos
Autores principales: Iodice, Rosa, Ugga, Lorenzo, Aruta, Francesco, Iovino, Aniello, Ruggiero, Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pacini Editore Srl 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315893/
https://www.ncbi.nlm.nih.gov/pubmed/32607477
http://dx.doi.org/10.36185/2532-1900-005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315893/
https://www.ncbi.nlm.nih.gov/pubmed/32607477
http://dx.doi.org/10.36185/2532-1900-005

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