{"id":12328,"date":"2024-10-11T23:20:13","date_gmt":"2024-10-11T21:20:13","guid":{"rendered":"https:\/\/valintermed.com\/?p=12328"},"modified":"2024-10-11T23:20:13","modified_gmt":"2024-10-11T21:20:13","slug":"okulotserebrokutannyy-sindrom","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/ocular-serebrovascular-accident\/","title":{"rendered":"Oculocerebrocutaneous syndrome"},"content":{"rendered":"
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Oculocerebrocutaneous syndrome (OCCS) is a rare genetic disorder characterized by tumors, eye abnormalities, and developmental abnormalities in other systems and organs, including the central nervous system. The main component of this syndrome is vascular abnormalities and neoplasms, which can manifest as hemiangiomas, hemangiopericomas, or other vascular lesions. OCCS can occur as an isolated condition or in combination with other hereditary syndromes, making its diagnosis and treatment difficult. An important aspect of this disease is the diversity of clinical manifestations and the need for an individual approach to each patient.<\/p>\n

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