{"id":13059,"date":"2024-08-23T05:55:37","date_gmt":"2024-08-23T03:55:37","guid":{"rendered":"https:\/\/valintermed.com\/?p=13059"},"modified":"2024-08-23T05:55:37","modified_gmt":"2024-08-23T03:55:37","slug":"spinotserebellyarnaya-ataksiya-tip-13","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/spinal-cord-injury-tip-13\/","title":{"rendered":"Spinocerebellar ataxia type 13"},"content":{"rendered":"
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Spinocerebellar ataxia type 13 (SCA13) is an inherited neurodegenerative disorder belonging to the group of spinocerebellar ataxias, characterized by progressive atrophy of the cerebellum and other structures of the central nervous system. The main manifestations of the disease include impaired motor coordination, ataxia, balance deficits, and severe dysfunction of the extrapyramidal system. These symptoms result from damage to the cerebellum, which plays a key role in regulating movement and maintaining balance. Although the severity of symptoms can vary, SCA13 typically results in a significant deterioration in the quality of life and loss of independence in patients as the disease progresses, affecting their motor skills and basic functions.<\/p>\n

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