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WHAT IS CHORIONIC VILLUS BIOPSY? HOW IS CHORIONIC VILLUS BIOPSY PERFORMED?
For expectant mothers, the health of their babies is always very important. Chorionic villus biopsy, which means taking a sample to be tested during pregnancy, is also among the subjects investigated by expectant mothers. So, what is a chorionic villus biopsy? How is chorionic villus biopsy performed? Here are the answers to those questions that mothers are wondering.
What is chorionic villus biopsy? How is chorionic villus biopsy performed? such questions are among the topics investigated by expectant mothers. What is chorionic villus biopsy (CVS), a procedure applied to expectant mothers before birth? How is chorionic villus biopsy (CVS) performed? Here are the answers to the curious questions.
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WHAT IS CHORIONIC VILLUS BIOPSY (CVS)?
Chorionic villi refers to a portion of the developing placenta. A chorionic villus biopsy is the taking of small amounts of chorionic villus samples to perform genetic testing at the stage of pregnancy. It’s a diagnostic test. It is applied to detect various genetic diseases and to test the baby’s chromosomes. 10 to 13. it is applied between Weeks.
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HOW IS CHORIONIC VILLUS BIOPSY (CVS) PERFORMED?
In the CVS process in Antalya JCI Hospital, a tissue sample is taken from the placenta, that is, the baby’s partner. The genetic makeup of the placenta is the same as the baby. First, the baby and placenta are checked with ultrasound. It is then passed through the skin and uterine wall located in the abdominal area with a thin needle and entered into the placenta. Then the desired tissue is taken.The tiny tissue taken does not cause any harm to the placenta or baby. The procedure does not require operating room conditions. It takes about 10-15 min. A tissue sample is sent to the lab.
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IN WHAT CASES IS CHORIONIC VILLUS BIOPSY (CVS) NECESSARY?
If a woman or man has a genetic disease that can be passed on to a child,
If there are genetic diseases in the family of a woman or man,
If you are having a genetic child in Turkey,
If tests conducted during pregnancy have determined that the child is at risk for a genetic disease.
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