Primary Progressive Multiple Sclerosis in a Portuguese Patient With Neurofibromatosis Type 1

Neurofibromatosis type 1 (NF1) is a frequent genetic neurocutaneous syndrome and multiple sclerosis (MS) is an acquired demyelinating disease of the central nervous system. The association of both these diseases is rare. In this case report, we describe a 25-year-old man with gait impairment, upper...

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Detalles Bibliográficos
Autores principales: Carvalho, Inês, Quintas-Neves, Miguel, Pinto, Joana, Santos, Ana Filipa, Pereira, João
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771896/
https://www.ncbi.nlm.nih.gov/pubmed/35103140
http://dx.doi.org/10.7759/cureus.20561

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771896/
https://www.ncbi.nlm.nih.gov/pubmed/35103140
http://dx.doi.org/10.7759/cureus.20561

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