{"id":11634,"date":"2025-07-26T09:24:43","date_gmt":"2025-07-26T07:24:43","guid":{"rendered":"https:\/\/valintermed.com\/?p=11634"},"modified":"2025-07-26T09:24:43","modified_gmt":"2025-07-26T07:24:43","slug":"sindrom-gemi-3","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/syndrome-gemi-3\/","title":{"rendered":"Hemi Syndrome 3"},"content":{"rendered":"
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Hemi syndrome 3 (or Hemi-3 syndrome) is a rare genetic disorder characterized by significant disruption of the central nervous system, as well as multiple anomalies in various organ systems. The most pronounced clinical manifestations include impaired motor function, mental retardation, seizures, as well as a number of serious developmental anomalies that can manifest in childhood. The disease is caused by mutations in genes responsible for the formation and functioning of neural circuits, and can lead to serious consequences for the patient, including the need for constant medical supervision and support. <\/p>\n

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