Multiple Sclerosis in Charcot-Marie-Tooth Disease Type 1A - A Case Report and Literature Review

Wen Yang1, Lei Zhou2, Gavin P Reynolds3

  • 1Puer People's Hospital, Puer, Yunnan, China.

Summary

Central nervous system (CNS) demyelination is rare in Charcot-Marie-Tooth disease (CMT). This case study explores a rare instance of CNS demyelination in CMT type 1A, suggesting a link to PMP22 gene mutations.