SCA-6 (SPINOCEREBELLAR ATAXIA), CACNA1A GENE MUTATION
SCA6 is an autosomal dominant ataxia with vibratory & proprioceptive sensory loss. It manifests later in life and is associated with cerebellar degeneration. In SCA 6 there is a CAG trinucleotide repeat in chromosome 19p which results in abnormal CACNA1A protein. Missense mutations in the same gene cause Familial hemiplegic migraine while nonsense mutations result in Hereditary paroxysmal cerebellar ataxia or Episodic ataxia.
Parameter(s) covered : 3
Report Frequency: Sample Tue by 11 am; Report Sat
Special Instruction: Physician prescription is mandatory.
Price : ₹ 2700.00
Parameters
- CACNA1A Gene CAG repeats Allele 1
- CACNA1A Gene CAG repeats Allele 2
- SCA-6