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Infantile Onset of Spinocerebellar Ataxia Type 5 (SCA-5) in a 6 Month Old with Ataxic Cerebral Palsy.

Gillian ReaSandya TirupathiJonathan WilliamsPenny CloustonPatrick John Morrison
Published in: Cerebellum (London, England) (2020)
Spinocerebellar ataxia type 5 (SCA-5) is a predominantly slowly progressive adult onset ataxia. We describe a child with a presentation of ataxic cerebral palsy (CP) and developmental delay at 6 months of age. Genetic testing confirmed a c.812C>T p.(Thr271Ile) mutation within the SPTBN2 gene. Seven previous cases of infantile onset SCA-5 are reported in the literature, four of which had a CP presentation. Early onset of SCA-5 presents with ataxic CP and is a rare cause of cerebral palsy.
Keyphrases
  • cerebral palsy
  • early onset
  • late onset
  • systematic review
  • multiple sclerosis
  • copy number
  • genome wide
  • gene expression
  • african american