{"id":13441,"date":"2024-08-22T23:30:47","date_gmt":"2024-08-22T21:30:47","guid":{"rendered":"https:\/\/valintermed.com\/?p=13441"},"modified":"2024-08-22T23:30:47","modified_gmt":"2024-08-22T21:30:47","slug":"h-stseplennyy-infantilnyy-nistagm","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennyy-infantilnyy-nistagm\/","title":{"rendered":"X-linked infantile nystagmus"},"content":{"rendered":"
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X-linked infantile nystagmus (XLN) is an inherited disorder characterized by characteristic eye movements that occur involuntarily. The disorder is controlled by genetic factors and the architecture of the nervous system. XLN typically begins in infancy, often within the first few months of life, and can be associated with significant vision problems. The main manifestations of the disorder are rhythmic oscillatory eye movements that can make focusing difficult and contribute to corrective problems with perceptual processing. Any intervention to correct the symptoms requires a multidisciplinary approach, including neurological, ophthalmological, and genetic interventions.<\/p>\n

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