SCA-1 (SPINOCEREBELLAR ATAXIA), ATXN1 GENE MUTATION
SCA1 is an autosomal dominant ataxia which manifests in early or middle adult life. It is characterized by progressive cerebellar ataxia of trunk & limbs, gait impairment, slow voluntary movements, scanning speech, tremors & nystagmoid eye movements. In SCA 1 there is a CAG trinucleotide repeat in chromosome 6p which gets affected & results in abnormal Ataxin-1 protein production.
Parameter(s) covered : 1
Report Frequency: Sample Tue by 11 am; Report Sat
Special Instruction: Physician prescription is mandatory.
Price : ₹ 2700.00
Parameters
- SCA-1