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Cerebral white matter abnormalities in patients with charcot-marie-tooth disease.
Lee, Mina; Park, Chang-Hyun; Chung, Hwa-Kyung; Kim, Hyeon Jin; Choi, Yunseo; Yoo, Jeong Hyun; Yoon, Young Chul; Hong, Young Bin; Chung, Ki Wha; Choi, Byung-Ok; Lee, Hyang Woon.
Afiliação
  • Lee M; Department of Neurology, Ewha Womans University School of Medicine and Ewha Medical Research Institute, Seoul, South Korea.
  • Park CH; Department of Medical Science, Ewha Womans University School of Medicine and Ewha Medical Research Institute, Seoul, South Korea.
  • Chung HK; Department of Neurology, Ewha Womans University School of Medicine and Ewha Medical Research Institute, Seoul, South Korea.
  • Kim HJ; Department of Medical Science, Ewha Womans University School of Medicine and Ewha Medical Research Institute, Seoul, South Korea.
  • Choi Y; Department of Neurology, Ewha Womans University School of Medicine and Ewha Medical Research Institute, Seoul, South Korea.
  • Yoo JH; Department of Neurology, Ewha Womans University School of Medicine and Ewha Medical Research Institute, Seoul, South Korea.
  • Yoon YC; Department of Neurology, Ewha Womans University School of Medicine and Ewha Medical Research Institute, Seoul, South Korea.
  • Hong YB; Department of Medical Science, Ewha Womans University School of Medicine and Ewha Medical Research Institute, Seoul, South Korea.
  • Chung KW; Department of Radiology, Ewha Womans University School of Medicine and Ewha Medical Research Institute, Seoul, South Korea.
  • Choi BO; Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
  • Lee HW; Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Ann Neurol ; 81(1): 147-151, 2017 Jan.
Article em En | MEDLINE | ID: mdl-27863451
ABSTRACT
Here, we report the structural evidence of cerebral white matter abnormalities in Charcot-Marie-Tooth (CMT) patients and the relationship between these abnormalities and clinical disability. Brain diffusion tensor imaging (DTI) was performed in CMT patients with demyelinating (CMT1A/CMT1E), axonal (CMT2A/CMT2E), or intermediate (CMTX1/DI-CMT) peripheral neuropathy. Although all patients had normal brain magnetic resonance imaging, all genetic subgroups except CMT1A had abnormal DTI findings indicative of significant cerebral white matter abnormalities decreased fractional anisotropy and axial diffusivity, and increased radial diffusivity. DTI abnormalities were correlated with clinical disability, suggesting that there is comorbidity of central nervous system damage with peripheral neuropathy in CMT patients. ANN NEUROL 2017;81147-151.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Doenças do Sistema Nervoso Periférico / Substância Branca Tipo de estudo: Observational_studies Limite: Female / Humans / Male Idioma: En Revista: Ann Neurol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Coréia do Sul

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Doenças do Sistema Nervoso Periférico / Substância Branca Tipo de estudo: Observational_studies Limite: Female / Humans / Male Idioma: En Revista: Ann Neurol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Coréia do Sul