Aktan, ZehraAkcakaya, Nihan HandeTekturk, PinarDeniz, EnginKoyuncu, BaharYapici, Zuhal2024-07-122024-07-1220180028-384310.1016/j.pjnns.2017.10.0162-s2.0-85033798343https://dx.doi.org/10.1016/j.pjnns.2017.10.016https://hdl.handle.net/20.500.12415/8372Charcot-Marie-Tooth (CMT) disease is a hereditary neurologic disease which affects the sensorial and motor fibers of the peripheral nerves. CMTX1 is an X-linked dominantly inherited subtype of CMT and is caused by mutations in gap junction beta 1 gene (GJB1). A small proportion of GJB1 mutations are associated with recurrent central nervous system findings. We describe a 15-year-old male patient with CMTX1 who had stroke-like findings along with foot deformities and peripheral neuropathy. Strokes and stroke-like attacks are rarely seen in children and adolescents. Herein, neurological signs, MRI findings and genetic results of a CMTX1 case are presented and discussed. (c) 2017 Polish Neurological Society. Published by Elsevier Sp. z o.o. All rights reserved.eninfo:eu-repo/semantics/closedAccessTransient ischemic-attack-likeStroke-likeCMTX1GJB1Pes cavusArticle288229153916Q228552WOS:000428392000025Q4