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Nervous system

Location>Home>Nervous system>N023:SCA dynamic mutation


     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.

     SCA dynamic mutation(SCA1,SCA2,SCA3,SCA6,SCA7,SCA8,SCA12,SCA17)