{"id":12801,"date":"2024-10-11T15:36:12","date_gmt":"2024-10-11T13:36:12","guid":{"rendered":"https:\/\/valintermed.com\/?p=12801"},"modified":"2024-10-11T15:36:12","modified_gmt":"2024-10-11T13:36:12","slug":"retinohoroidalnaya-koloboma","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/retinohoroid-coloboma\/","title":{"rendered":"Retinochoroidal coloboma"},"content":{"rendered":"
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Retinochoroidal coloboma is a congenital defect that affects the retina and choroid of the eye. This disease is characterized by the absence or underdevelopment of certain areas of the retina and choroid, which can lead to various visual impairments, including amblyopia and decreased visual acuity. Coloboma can vary in size and location - from small changes to significant defects in the macula and optic disc. Depending on the location of the coloboma, patients may experience both limited peripheral and central vision. This pathology is often associated with other anomalies, such as glaucoma and developmental defects of the spectrum of the brain, which predetermines its multifactorial nature of occurrence.<\/p>\n

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