SCA-2 (SPINOCEREBELLAR ATAXIA), ATXN2 GENE MUTATION

Spinocerebellar ataxia (SCA) or also known as Spinocerebellar atrophy or Spinocerebellar degeneration, is a progressive, degenerative genetic disease with multiple types. In SCA 2 there is a CAG trinucleotide repeat in chromosome 12q which gets affected which results in abnormal Ataxin 2 protein production

  • Test Type:
  • Pre-test Information:
  • Report Delivery:
    Sample by Tue 11 am; Report Sat
  • Components:
    0