A rare association between multiple sclerosis and Charcot‐Marie‐Tooth type 1B

The association between multiple sclerosis (MS) and hereditary and sporadic demyelinating disorders of the peripheral nervous system is extremely rare. We herein report a case of Charcot‐Marie‐Tooth disease type 1B with p.Val102fs mutation in the MPZ gene that developed relapsing remitting MS. [Imag...

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Detalles Bibliográficos
Autores principales: Cortese, Rosa, Zoccolella, Stefano, Muglia, Maria, Patitucci, Alessandra, Scarafino, Antonio, Paolicelli, Damiano, Simone, Isabella Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Commentary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167010/
https://www.ncbi.nlm.nih.gov/pubmed/28032003
http://dx.doi.org/10.1002/brb3.580

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167010/
https://www.ncbi.nlm.nih.gov/pubmed/28032003
http://dx.doi.org/10.1002/brb3.580

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