SCA-8 (SPINOCEREBELLAR ATAXIA), ATXN8OS & ATXN8 GENE MUTATION
SCA8 is an autosomal dominant slowly progressive ataxia with dysarthria. It usually manifests at 40 years of age with a range from 20 to 65 years. Other features include nystagmus, leg spasticity & reduced vibratory sensation. SCA8 is caused by bidirectional transcription at the SCA8 locus on chromosome 13q21 involving both an expanded CTG trinucleotide repeat in the ATXN8OS gene and the complementary CAG repeat in the ATXN8 gene (13q21).
Parameter(s) covered : 3
Report Frequency: Sample Tue by 11 am; Report Sat
Special Instruction: Physician prescription is mandatory.
Price : ₹ 6000.00
Parameters
- ATXN8OS/ATXN8 Gene Repeats Allele 1
- ATXN8OS/ATXN8 Gene Repeats Allele 2
- SCA-8