S0011
SCA 17 (Spinocerebellar Ataxia Type-17)
Test Details: SCA 17 is an autosomal dominant neurological disorder. It is characterized by ataxia, dementia, involuntary movements. The diagnosis of SCA17 is established in a proband by identification of an abnormal CAG/CAA repeat expansion in TBP gene.
Category
Molecular Genetics
Pre-test Information
Clinical details & history is mandatory.
Report Delivery
8 working days
Gender
All
Organ
Nervous System
SCA 17 (Spinocerebellar Ataxia Type-17)
2900
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