{"id":12382,"date":"2024-10-11T22:32:39","date_gmt":"2024-10-11T20:32:39","guid":{"rendered":"https:\/\/valintermed.com\/?p=12382"},"modified":"2024-10-11T22:32:39","modified_gmt":"2024-10-11T20:32:39","slug":"sindrom-ohdo-variant-seya-barbera-bisekera-yanga-simpsona","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/sindrom-ohdo-variant-seya-barbera-bisekera-yanga-simpsona\/","title":{"rendered":"Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant"},"content":{"rendered":"
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Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant, is a rare genetic disorder characterized by a variety of clinical manifestations, including optical, congenital and developmental anomalies. This condition belongs to a group of syndromes associated with chromosome anomalies, and is particularly associated with mutations in genes responsible for the development of various organs and systems. The most common symptoms include intellectual disability, limb anomalies, dental anomalies, and specific facial features. It is important to note that this disease has a complex pathogenesis and varies in severity, which makes it difficult to diagnose and manage.<\/p>\n

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