{"id":13278,"date":"2024-08-23T02:16:32","date_gmt":"2024-08-23T00:16:32","guid":{"rendered":"https:\/\/valintermed.com\/?p=13278"},"modified":"2024-09-21T18:08:30","modified_gmt":"2024-09-21T16:08:30","slug":"triploidiya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/triploidiya\/","title":{"rendered":"Triploidy"},"content":{"rendered":"
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Triploidy is a chromosomal disorder characterized by the presence of a triple set of chromosomes (69 chromosomes instead of the normal 46). This abnormality occurs as a result of an error in cell division, which results in the zygote receiving three copies of all the chromosomes from its parents. Triploidy can be polyploid (coming from both parental cells) or aneuploid. Because the excess amount of genetic material disrupts normal development, triploidy often results in miscarriage or the birth of children with severe pathology. Characteristic manifestations can include physical abnormalities such as microcephaly and severe organ dysfunction. Unfortunately, live birth of a child with triploidy is rare, and many of these cases end in intrauterine fetal death.<\/p>\n

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