Pregnant women and mothers have all experienced that maintaining pregnancy is not as simple as they say, and the process of pregnancy is not as smooth as everyone thinks. During pregnancy, a lot of examinations need to be done to check the health of the fetus and the mother. The early stages of pregnancy are the most dangerous days during the tenth month of pregnancy, and pregnant mothers need to pay extra attention. So what can be detected by embryonic villus chromosome examination?
Embryo chorionic villi chromosome examination, also known as chorionic villi penetration, is a chromosomal examination performed by removing the villi through the vagina or abdomen after 50 days of pregnancy. It mainly checks whether the fetus has chromosomal diseases or hidden genetic diseases, such as Down syndrome, Mediterranean anemia, etc. However, this examination can cause great harm to both the mother and the fetus, and can easily lead to miscarriage, physical disabilities, congenital heart disease, congenital gastrointestinal disease, congenital kidney disease, and so on, with a very high risk of onset.
Even pregnant women who have had an abortion need to undergo embryo chorionic chromosome testing to prevent further miscarriages. In addition, for individuals with production dysfunction, abnormal secondary sexual characteristics, abnormal external reproductive organs, congenital genetic diseases, and intellectual disabilities, embryo chorionic chromosome examination is necessary to determine whether the fetus in the abdomen can grow healthily.
