Amniocentesis treatment is done to check a kind of DNA, or deoxyribonucleic acid, which is the hereditary material that determines the inheritance of eye colour, hair colour, stature, bone density and many other human and animal traits. The information in DNA is stored as a code made up of four nucleotide bases: adenine (A), guanine (G), cytosine (C), and thymine (T). DNA is organised into long structures called chromosomes. These chromosomes are duplicated before cells divide. Human beings contain 46 DNA molecules. A sexologist to help determine different kinds of chromosomal and genetic disorders in the foetus does it.
The prenatal sex discernment is the most accurate technology available for determining paternity and other family relationships. The testing procedure can take about 20-30 minutes post which you have to await the results. First, is method is Amniocentesis. In this doctor uses ultrasound to guide a thin needle into the uterus. The needle draws out a small amount of amniotic fluid, which is tested. The second method is Chorionic Villus Sampling (CVS).
If the amniotic fluid shows signs of some kind of chromosomal or genetic disorder problem. If that is the case then the doctor would either suggest abortion or some alternative therapy. In other cases, prenatal treatment is done to ensure that such genes are not passed on from the parents to the child, thus reducing risks of abnormalities.