{"id":12300,"date":"2024-10-11T23:54:22","date_gmt":"2024-10-11T21:54:22","guid":{"rendered":"https:\/\/valintermed.com\/?p=12300"},"modified":"2024-10-11T23:54:22","modified_gmt":"2024-10-11T21:54:22","slug":"glazodvigatelnaya-apraksiya-tipa-kogana","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/cog-type-ocular-motor-apraxia\/","title":{"rendered":"Oculomotor apraxia of the Kogan type"},"content":{"rendered":"
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Cogan's oculomotor apraxia is a complex neurological disorder associated with impaired voluntary eye movement with preserved functionality. This disorder manifests itself in difficulty in purposeful eye movement despite normal vision and ocular structure. The main problem is that the patient cannot initiate eye movements, although the eyes remain intact and undamaged. This disorder is often observed in combination with other neurological symptoms and may indicate the presence of diseases of the central nervous system. Oculomotor apraxia can be caused by various factors, including vascular disorders, head injuries, tumors, and neurodegenerative conditions.<\/p>\n

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