{"id":13160,"date":"2024-08-23T04:15:01","date_gmt":"2024-08-23T02:15:01","guid":{"rendered":"https:\/\/valintermed.com\/?p=13160"},"modified":"2024-08-23T04:15:01","modified_gmt":"2024-08-23T02:15:01","slug":"mozaitsizm-trisomii-3","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/trisomiasis-mosaicism-3\/","title":{"rendered":"Trisomy 3 mosaicism"},"content":{"rendered":"
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Trisomy 3, also known as trisomy 3 mosaicism, is a genetic disorder in which an extra third chromosome is present in some cells of the body, causing a variety of developmental disabilities. The condition can occur in both mosaic and non-mosaic forms, with mosaicism involving the presence of normal cells alongside cells that have the third chromosome. Symptoms of trisomy 3 vary depending on the number and distribution of cells with the abnormal chromosome and can include physical, neurological, and cognitive impairment. Most cases of trisomy 3 are congenital and can be detected either during pregnancy or after birth, but many children with mosaicism have normal or near-normal development and physical fitness.<\/p>\n

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