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
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author Cortese, Rosa
Zoccolella, Stefano
Muglia, Maria
Patitucci, Alessandra
Scarafino, Antonio
Paolicelli, Damiano
Simone, Isabella Laura
author_facet Cortese, Rosa
Zoccolella, Stefano
Muglia, Maria
Patitucci, Alessandra
Scarafino, Antonio
Paolicelli, Damiano
Simone, Isabella Laura
author_sort Cortese, Rosa
collection PubMed
description 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. [Image: see text]
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spelling pubmed-51670102016-12-28 A rare association between multiple sclerosis and Charcot‐Marie‐Tooth type 1B Cortese, Rosa Zoccolella, Stefano Muglia, Maria Patitucci, Alessandra Scarafino, Antonio Paolicelli, Damiano Simone, Isabella Laura Brain Behav Commentary 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. [Image: see text] John Wiley and Sons Inc. 2016-09-25 /pmc/articles/PMC5167010/ /pubmed/28032003 http://dx.doi.org/10.1002/brb3.580 Text en © 2016 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Cortese, Rosa
Zoccolella, Stefano
Muglia, Maria
Patitucci, Alessandra
Scarafino, Antonio
Paolicelli, Damiano
Simone, Isabella Laura
A rare association between multiple sclerosis and Charcot‐Marie‐Tooth type 1B
title A rare association between multiple sclerosis and Charcot‐Marie‐Tooth type 1B
title_full A rare association between multiple sclerosis and Charcot‐Marie‐Tooth type 1B
title_fullStr A rare association between multiple sclerosis and Charcot‐Marie‐Tooth type 1B
title_full_unstemmed A rare association between multiple sclerosis and Charcot‐Marie‐Tooth type 1B
title_short A rare association between multiple sclerosis and Charcot‐Marie‐Tooth type 1B
title_sort rare association between multiple sclerosis and charcot‐marie‐tooth type 1b
topic Commentary
url 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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