{"id":13454,"date":"2024-08-22T23:00:56","date_gmt":"2024-08-22T21:00:56","guid":{"rendered":"https:\/\/valintermed.com\/?p=13454"},"modified":"2024-08-22T23:21:00","modified_gmt":"2024-08-22T21:21:00","slug":"sindrom-deletsii-3p","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/deletii-syndrome-3p\/","title":{"rendered":"3p deletion syndrome"},"content":{"rendered":"
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3p deletion syndrome, also known as Christenson syndrome, is a rare genetic disorder caused by the loss of a portion of the short arm of chromosome 3. This condition often results in multiple phenotypic manifestations, including mental retardation, growth retardation, and various physical anomalies. Symptoms can vary, making diagnosis difficult and requiring an individual approach to each patient. The severity of the syndrome depends on the size and location of the deletion, as well as the genes involved. The syndrome was first reported in clinical practice in the late 20th century, when scientists began to identify links between genetic disorders and phenotypic traits. <\/p>\n

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