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.
A rare association between multiple sclerosis and Charcot-Marie-Tooth type 1B
CORTESE, ROSA;ZOCCOLELLA, STEFANO;SCARAFINO, ANTONIO;PAOLICELLI, DAMIANO;SIMONE, Isabella Laura
2016-01-01
Abstract
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.File in questo prodotto:
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