{"id":13453,"date":"2024-08-22T23:01:20","date_gmt":"2024-08-22T21:01:20","guid":{"rendered":"https:\/\/valintermed.com\/?p=13453"},"modified":"2024-08-22T23:10:42","modified_gmt":"2024-08-22T21:10:42","slug":"sindrom-deletsii-2q37","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/deletii-syndrome-2q37\/","title":{"rendered":"2q37 deletion syndrome"},"content":{"rendered":"
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2q37 deletion syndrome is a rare genetic disorder characterized by the loss of a fragment of chromosome 2 on the long arm at 2q37. The disorder results from a deletion that results in a variety of manifestations, including intellectual disability, developmental delay, physical developmental abnormalities, and various associated medical conditions. Symptoms may vary from patient to patient, making diagnosis difficult and requiring an individualized approach to treatment. In this context, pathological manifestations may include neurological disorders, organ dysfunction, and characteristic facial features, all of which are due to abnormalities in the genetic code.<\/p>\n

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