Neuromyelitis Optica Spectrum Disorder Coinciding with Spinocerebellar Ataxia Type 31

We report the unusual case of a 63-year-old man with spinocerebellar ataxia (SCA) type 31 who developed neuromyelitis optica spectrum disorder (NMOSD) 14 years after the onset of cerebellar symptoms. In addition to cerebellar atrophy, magnetic resonance imaging showed multiple high-intensity areas i...

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Detalhes bibliográficos
Main Authors: Yoshiaki Takahashi, Yasuhiro Manabe, Ryuta Morihara, Hisashi Narai, Toru Yamashita, Koji Abe
Formato: Artigo
Idioma:Inglês
Publicado em: Karger Publishers 2017-05-01
Colecção:Case Reports in Neurology
Assuntos:
Neuromyelitis optica spectrum disorder
Anti-aquaporin-4 antibody
Spinocerebellar ataxia type 31
Neurodegeneration
Autoimmune disease
Central nervous system disease
Acesso em linha:http://www.karger.com/Article/FullText/475657
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