SCA-11 (SPINOCEREBELLAR ATAXIA), TTBK2 GENE MUTATION
SCA11 is a subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the early-onset of cerebellar signs, eye movement abnormalities and pyramidal signs. ADCA III is an autosomal dominant cerebellar ataxia, relatively benign, late-onset, slowly progressive neurologic disorder characterized by an uncomplicated cerebellar syndrome. SCA11 is characterized by progressive cerebellar ataxia and abnormal eye signs (jerky pursuit, horizontal and vertical nystagmus). Pyramidal features, peripheral neuropathy and dystonia are seen occasionally. This test targets the exon 12 of TTBK2 gene.
Parameter(s) covered : 1
Report Frequency: Sample Tue by 11 am; Report Sat
Special Instruction: Physician prescription is mandatory.
Price : ₹ 5900.00
Parameters
- TTBK2 Gene Mutation