{"id":12329,"date":"2024-10-11T23:32:24","date_gmt":"2024-10-11T21:32:24","guid":{"rendered":"https:\/\/valintermed.com\/?p=12329"},"modified":"2024-10-11T23:32:24","modified_gmt":"2024-10-11T21:32:24","slug":"olivopontotserebellyarnaya-atrofiya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/olivopontotserebellyarnaya-atrophiya\/","title":{"rendered":"Olivopontocerebellar atrophy"},"content":{"rendered":"
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Olivo-pontocerebellar atrophy (OPCA) is a rare neurodegenerative disorder that belongs to the group of hereditary ataxias. It is characterized by progressive destruction of neurons in the olivary, pontine, and cerebellar regions, leading to impaired coordination of movements, dysartery, and a number of other neurological symptoms. The disease can manifest itself in various forms, ranging from balance disorders to more severe disorders. Clinical and genetic studies have established that OPCA can manifest itself both in hereditary forms and in sporadic cases without a previous hereditary load, expanding this area of study in modern neurology.<\/p>\n

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