{"id":12978,"date":"2024-08-23T07:16:27","date_gmt":"2024-08-23T05:16:27","guid":{"rendered":"https:\/\/valintermed.com\/?p=12978"},"modified":"2024-08-23T07:16:27","modified_gmt":"2024-08-23T05:16:27","slug":"sindrom-stuve-videmanna","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/stuve-videmanna-syndrome\/","title":{"rendered":"Stuve-Wiedemann syndrome"},"content":{"rendered":"
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Stuve-Wiedemann syndrome is a rare genetic disorder that belongs to a group of disorders with manifestations in various systems and organs. The main clinical manifestations of the syndrome include multiple skeletal abnormalities, neurological disorders, as well as narrowing of the omental veins and hernias. The disease has a complex pathophysiological mechanism, including disorders in the development of bone and nervous tissue, which leads to the formation of characteristic signs. The syndrome is inherited in an autosomal recessive manner, which requires the identification of carriers of maut genes for the prevention and early diagnosis of the disease.<\/p>\n

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