{"id":13056,"date":"2024-08-23T05:56:57","date_gmt":"2024-08-23T03:56:57","guid":{"rendered":"https:\/\/valintermed.com\/?p=13056"},"modified":"2024-08-23T05:56:57","modified_gmt":"2024-08-23T03:56:57","slug":"spinotserebellyarnaya-ataksiya-tip-10","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/spinal-cord-injury-tip-10\/","title":{"rendered":"Spinocerebellar ataxia type 10"},"content":{"rendered":"
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Spinocerebellar ataxia type 10 (SCA10) is an inherited neurodegenerative disorder belonging to the group of spinocerebellar ataxias, characterized by progressive motor incoordination, static and dynamic ataxia, and neurological deficits such as dysarthria and nystagmus. These symptoms result from degeneration of neurons in the cerebellum and spinal tracts. The disease is generally considered dominantly inherited and is associated with the expansion of repetitive nucleotide sequences in the ATXN10 gene, leading to protein dysfunction and subsequent neurological destruction.<\/p>\n

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