{"id":13450,"date":"2024-08-22T23:02:16","date_gmt":"2024-08-22T21:02:16","guid":{"rendered":"https:\/\/valintermed.com\/?p=13450"},"modified":"2024-08-22T23:19:41","modified_gmt":"2024-08-22T21:19:41","slug":"sindrom-3mc","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/sindrom-3mc\/","title":{"rendered":"3MC Syndrome"},"content":{"rendered":"
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3MC syndrome (full name - 3M syndrome) is a rare genetic disorder characterized by specific developmental disorders, mainly associated with head and face anomalies, as well as growth and mental retardation. The main manifestations of the syndrome may include tissue dysplasia, decreased skull size (microcephaly), dental formation disorders, and various limb anomalies. These clinical manifestations are explained by the presence of a hereditary predisposition associated with changes in the genes responsible for the synthesis of proteins that participate in the development and formation of the body at the cellular level.<\/p>\n

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