Chromosomal abnormalities result in more than 50% of miscarriages in the early stages of pregnancy. Abnormalities affecting the fetus are known as chromosomal abnormalities. An attempt to detect these abnormalities in the earlier stages of pregnancy is done with the help of various screening tests. These tests are usually advised to be taken, by gynaecologists if they find any abnormal pregnancy symptoms. Post chromosomal abnormality screening treatments are not possible. It is only possible to detect the abnormalities and get prepared to face the same. The most common type of screening is AFP screening. The level, if higher or lower than normal indicates that there might be an abnormality. If the level is lower it means that the child may have low IQ, short limbs and/ or might be prone to heart diseases and if the level is higher the child may have a neural tube defect. Ultrasound, Quad screen, Triple screen and Chorionic Villus Sampling are other screening tests which are used to detect any defects. Maternal blood screening is another common test performed to find out if there is a risk of any abnormalities. A molar pregnancy test is done to find out if there is an abnormal composition of a chromosome. This is done with the help of repetitive urine tests and is done to ensure disappearance of hCG in the urine. All these tests are however not conclusive in nature.
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