SCA-23 (SPINOCEREBELLAR ATAXIA), PDYN GENE MUTATION
SCA23 is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). ADCA I is characterized by cerebellar ataxia in combination with various associated neurologic features, such as ophthalmoplegia, pyramidal and extrapyramidal signs, peripheral neuropathy and dementia among others. SCA-23 is an adult-onset neurodegenerative disorder characterized by slowly progressive gait and limb ataxia, with variable additional features, including peripheral neuropathy and dysarthria. Majority are caused by heterozygous mutations in exon 4 of PDYN gene.
Parameter(s) covered : 1
Report Frequency: Sample Tue by 11 am; Report Sat
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Price : ₹ 6000.00
Parameters
- PDYN Gene Mutation