{"id":11431,"date":"2025-07-26T19:28:24","date_gmt":"2025-07-26T17:28:24","guid":{"rendered":"https:\/\/valintermed.com\/?p=11431"},"modified":"2025-07-26T19:28:24","modified_gmt":"2025-07-26T17:28:24","slug":"sindrom-tsefalopolisindaktilii-greyga","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/tsefalopolis-sindactylii-grayga\/","title":{"rendered":"Greig's cephalopolysyndactyly syndrome"},"content":{"rendered":"
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Greig cephalopolysyndactyly syndrome (GCSS) is a rare genetic disorder characterized by a combination of various developmental anomalies. The main clinical manifestations of the syndrome are abnormalities in the formation of the skull, face, limbs, as well as the presence of digital syndactyly, which leads to disruption of normal functioning and aesthetics. This pathology may include micrognathia, underdevelopment or absence of individual fingers, and other changes that can vary significantly from patient to patient. The syndrome was first described in the medical literature in 1976, and since then scientists have conducted a significant amount of research aimed at studying it.<\/p>\n

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