{"id":12768,"date":"2024-10-11T16:05:08","date_gmt":"2024-10-11T14:05:08","guid":{"rendered":"https:\/\/valintermed.com\/?p=12768"},"modified":"2024-10-11T16:05:08","modified_gmt":"2024-10-11T14:05:08","slug":"pigmentnyy-retinit","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/pigmentary-retinitis\/","title":{"rendered":"Retinitis pigmentosa"},"content":{"rendered":"
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Pigmentary retinitis (pigment attack) is a hereditary disease of the retina, characterized by progressive deterioration of vision, which is associated with degeneration of photoreceptors, mainly rods, and subsequent decrease in the function of the visual analyzer. The main manifestations of the disease include night blindness, narrowing of the visual fields and, ultimately, possible blindness. Pigmentary retinitis can be caused by various gene mutations, which leads to metabolic disorders in the retina and degenerative processes that have a negative impact on vision.<\/p>\n

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