{"id":12692,"date":"2024-10-11T17:19:40","date_gmt":"2024-10-11T15:19:40","guid":{"rendered":"https:\/\/valintermed.com\/?p=12692"},"modified":"2024-10-11T17:19:40","modified_gmt":"2024-10-11T15:19:40","slug":"sindrom-pigmentnoy-dispersii","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/pigment-dispersive-syndrome\/","title":{"rendered":"Pigment dispersion syndrome"},"content":{"rendered":"
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Pigment dispersion syndrome is a hereditary eye disease characterized by abnormal dispersion of pigment in the iris, leading to increased intraocular pressure and, as a consequence, possible development of glaucoma. This condition is mainly associated with a disorder of melanin metabolism, which leads to its release into the anterior chamber of the eye and can cause obstruction of drainage pathways. The pathology is most often observed in young and middle age, and although clinical manifestations may be minor in the early stages, the progression of the disease leads to deterioration of vision and serious complications.<\/p>\n

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