{"id":11222,"date":"2025-07-27T05:55:43","date_gmt":"2025-07-27T03:55:43","guid":{"rendered":"https:\/\/valintermed.com\/?p=11222"},"modified":"2025-07-27T05:55:43","modified_gmt":"2025-07-27T03:55:43","slug":"semeynaya-ekssudativnaya-vitreoretinopatiya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/family-exsudativnoe-vitreoretinopatiya\/","title":{"rendered":"Familial exudative vitreoretinopathy"},"content":{"rendered":"
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Familial exudative vitreoretinopathy (FEVR) is a hereditary disease characterized by pathological changes in the posterior segment of the eye, including the retina and vitreous body. This condition primarily manifests itself as the formation of exudates in the retinal area, which can lead to significant visual impairment and, ultimately, blindness. The disease often begins to manifest itself in childhood and is progressive. The pathology is associated with impaired vascular permeability, which leads to the formation of edema and hemorrhages in the retina. An important feature of FEVR is its familial nature, which suggests a genetic predisposition and possible changes in many genes responsible for vascular regulation and metabolism in the eyes.<\/p>\n

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