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Coexistence of multiple sclerosis and spinocerebellar ataxia type-8.
Neyal, Nur; Keegan, B Mark; Kantarci, Orhun H; Zeydan, Burcu.
Afiliação
  • Neyal N; Nur Neyal Department of Radiology, Mayo Clinic, Rochester, MN, USA.
  • Keegan BM; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Kantarci OH; Center for Multiple Sclerosis and Autoimmune Neurology, Mayo Clinic, Rochester, MN, USA.
  • Zeydan B; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Mult Scler ; 29(9): 1195-1198, 2023 08.
Article em En | MEDLINE | ID: mdl-37401111
ABSTRACT
Cerebellar dysfunction is likely to cause severe and treatment-resistant disability in multiple sclerosis (MS). Certain spinocerebellar ataxia (SCA)-related alleles can increase MS susceptibility, and channel polymorphisms can impact disability measures. Following an index patient with the coexistence of MS and SCA Type-8 (SCA8) in the MS clinic, an institutional engine search for MS and hereditary ataxia coexistence was conducted but did not reveal any other cases. This extremely rare coexistence of MS and SCA8 in our index patient may be incidental; however, a yet-to-be-identified contribution of coexistent hereditary ataxia(s) to the susceptibility of a prominent progressive ataxia MS phenotype cannot be ruled out.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degenerações Espinocerebelares / Esclerose Múltipla Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Mult Scler Assunto da revista: NEUROLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degenerações Espinocerebelares / Esclerose Múltipla Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Mult Scler Assunto da revista: NEUROLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos