Price:
Rs. 3,390.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes: S0075
Frequently Asked Questions (FAQ's):
What is SCA17?
SCA17 is a hereditary neurodegenerative disorder caused by repeat expansion mutations in the TBP gene.
Why is this test done?
To confirm the genetic cause of suspected spinocerebellar ataxia and support clinical evaluation.
What sample is required?
EDTA blood is required for DNA extraction and analysis.
How is the test performed?
Advanced molecular methods, including PCR-based assays and fragment analysis, are used to detect TBP gene repeat expansions.
Is fasting needed before the test?
No, fasting or special preparation is not required.
Can this test help family members?
Yes, it assists in evaluating hereditary risk and is useful for genetic counselling in affected families.
What symptoms may suggest SCA17?
Ataxia, coordination problems, cognitive impairment, psychiatric symptoms, and involuntary movements.
Does Metropolis Healthcare offer this test?
Yes, Metropolis Healthcare provides accurate and reliable DNA-based testing for SCA17