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Chorionboholy Biopsy: What You Need to Know About Really Dangerous Examination

Chorionic bladder biopsy, that is, lung tissue sampling, is a small sample from the tissue of the lichen, which can be screened and analyzed to detect numerous genetic abnormalities.

Chorionboholy biopsy: what you need to know about roula?

Although primarily used to diagnose Down syndrome, it can be used to detect about 200 genetic defects. Chorionic fluff ensure that the larvae are connected to the maternal blood circulation at a higher surface area, meaning that the fetus can obtain more nutrients more efficiently. The Chorion Bohol Examination in Early Pregnancy, pp. 10-11. weekly, as opposed to amniocentesis, that is, amniocentesis, which is usually described in Figures 15-20. The purpose of chorionic bohol sampling is to screen for a variety of genetic disorders, particularly Down's syndrome (but many other disorders can also be detected). I recommend that you test themwho have a high risk of chromosome aberrations on the basis of first trimester genetic ultrasound, biochemistry, or genetic testing, who have had previous pregnancies, Genetic abnormalities increase in women over 35 years of age, the risk of Down syndrome, which is why they may be recommended for examination. Of course, the question of whether or not to pass the exam is seriously overlooked. During the examination, with ultrasound monitoring, a very small instrument is sampled from the bed. The exam is not painful, but it can be unpleasant. It is recommended to eat and drink before (especially drink - full bladder can improve the effectiveness of ultrasound examination).The major danger of chorionic bladder biopsy is abortion, although the probability is less than 1%. In addition, other problems may occur, such as leakage of amniotic fluid and the risk of infection. As a result, chorionic infestation may also slightly compromise fetal development. Another, quite terrific thing, is that the fetus may be injured during sampling, especially if the test is done very early (before week 10). Unfortunately, this can also have irreversible consequences, such as the loss of the fetal limb.There is also a harmless alternative State-of-the-art, non-invasive tests analyze maternal blood for the detection of genetic abnormalities. These tests take a few milliliters of blood from the mother, which is completely harmless to the fetus.
Such tests are available in Hungary, such as the combined test and the Nifty test, the former being able to detect fetal chromosome aberrations with 95% accuracy and within 100% accuracy.
A genetic abnormality screening based on a blood test is just worthwhile because it provides accurate, reassuring results, but is also much more rewarding for the fetus and the mother.

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