{"id":12380,"date":"2024-10-11T22:33:34","date_gmt":"2024-10-11T20:33:34","guid":{"rendered":"https:\/\/valintermed.com\/?p=12380"},"modified":"2024-10-11T22:33:34","modified_gmt":"2024-10-11T20:33:34","slug":"sindrom-omenna","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/omenna-syndrome\/","title":{"rendered":"Omenn syndrome"},"content":{"rendered":"
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Omenn syndrome is a rare but serious genetic disorder characterized by immune system disorders and dermatological manifestations. The syndrome was first described in 1965 and is associated with disorders in the T-lymphocyte system, which leads to the development of allopathic immunodeficiency, chronic infectious diseases and various dermatological problems. The most pronounced symptoms include exudative dermatitis, skin lesions, and systemic manifestations. The disease affects both children and adults and can have a different clinical spectrum.<\/p>\n

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