attention us:
Product Catalogue
Contact information
Welcome to call the service hotline



Nervous system

Location>Home>Nervous system>N022:SCA


 Spinocerebellar ataxia, cerebellar ataxia is a autosomal dominant genetic disease, that the main symptoms is cerebellar ataxia, such pathological changes in the cerebellum, spinal cord, brain stem degeneration. The main clinical features of the disease is cerebellar ataxia, and may be associated with dysarthria, tremor, pyramidal signs and dementia. Mygenostics is aimed to detect and analysis multiple subtypes of Spinocerebellar ataxia, cerebellar ataxia by hand in hand with clinical experts, combined with a new generation of high-throughput sequencing technology and bioinformatics analysis, to provide reliable basis for early diagnosis of Spinocerebellar ataxia, cerebellar ataxia patients.

     Spinal cord cerebellar ataxia related gene detects the panel + PCR dynamic mutation.