{"id":12323,"date":"2024-10-11T23:33:34","date_gmt":"2024-10-11T21:33:34","guid":{"rendered":"https:\/\/valintermed.com\/?p=12323"},"modified":"2024-10-11T23:33:34","modified_gmt":"2024-10-11T21:33:34","slug":"okulokutannyy-albinizm","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/oculocutaneous-albinism\/","title":{"rendered":"Oculocutaneous albinism"},"content":{"rendered":"
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Oculocutaneous albinism (OCA) is an inherited disorder characterized by a lack of pigmentation in the skin, hair, and eye, resulting in increased sensitivity to light and the risk of developing various visual impairments. The main cause of this disorder is a mutation in the genes associated with melanin production, which leads to insufficient or absent pigmentation in areas of the skin and hair, as well as in the iris of the eye. People with OCA often suffer from various ophthalmological disorders, such as nystagmus, astigmatism, and other types of refractive errors, which can significantly affect their quality of life.<\/p>\n

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