SCA-1 (SPINOCEREBELLAR ATAXIA), ATXN1 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 1 there is a CAG trinucleotide repeat in chromosome 6p which gets affected which results in abnormal Ataxin 1 protein production

  • Test Type:
  • Pre-test Information:
    Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
  • Report Delivery:
    Sample by Tue 11 am; Report Sat
  • Components:
    0