{"id":11915,"date":"2025-06-17T08:01:13","date_gmt":"2025-06-17T06:01:13","guid":{"rendered":"https:\/\/valintermed.com\/?p=11915"},"modified":"2025-06-17T08:01:13","modified_gmt":"2025-06-17T06:01:13","slug":"sindrom-legiusa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/legius-syndrome\/","title":{"rendered":"Legius syndrome"},"content":{"rendered":"
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Legius syndrome is a rare autosomal dominant genetic disorder characterized by multiple caf\u00e9 au lait spots, specific facial dysmorphia, and an increased risk of developing tumors. This pathology belongs to the group of neurofibromatosis-like disorders and is often accompanied by dysfunction of the central nervous system, including mental retardation of varying severity. The clinical picture of the disease is characterized by significant polymorphism of manifestations, which complicates timely diagnosis and requires a comprehensive approach to examining patients.<\/p>\n

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