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Coexistence of multiple sclerosis and spinocerebellar ataxia type-8.

Nur NeyalB Mark KeeganOrhun H KantarciBurcu Zeydan
Published in: Multiple sclerosis (Houndmills, Basingstoke, England) (2023)
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.
Keyphrases
  • multiple sclerosis
  • mass spectrometry
  • early onset
  • ms ms
  • white matter
  • primary care
  • gene expression
  • dna methylation
  • genome wide
  • single cell