Kurt, SemihaKaraer, HaticeKaplan, YukselAkat, IrernBattaloglu, EsraEruslu, DidernBasak, A. Nazli2024-08-042024-08-0420100022-510X1878-5883https://doi.org/10.1016/j.jns.2009.09.028https://hdl.handle.net/11616/94921Myotonic Dystrophy Type 1 (DM1) in combination with demyelinating neuropathy is very rare in literature. In this Study, DM1 and demyelinating neuropathy were demonstrated clinically and electromyographically in a 43-year-old female patient from Turkey. In the patient an expanded CTG repeat in the Myotonic Dystrophy Protein Kinase (DMPK) gene was confirmed in combination with a duplication in the Charcot-Marie-Tooth Disease (CMT1A) gene. DM1 was also determined in her 25-year-old son. (C) 2009 Elsevier B.V. All rights reserved.eninfo:eu-repo/semantics/closedAccessMyotonic dystrophyHereditary motor and sensory neuropathyCharcot-Marie-Tooth diseaseArticle2881-21971991984612010.1016/j.jns.2009.09.0282-s2.0-71049133503Q2WOS:000274042500035Q2