Noninvasive prenatal testing procedures, or NIPT tests, use a pregnant person's blood to find congenital DNA abnormalities in the fetus. DNA analysis is performed to check for genetic disorders like Down syndrome. Conditions cannot be diagnosed by NIPT tests. They communicate to your physician the likelihood that a condition is present. Starting around week ten of pregnancy, this test can be performed. Noninvasive prenatal testing is known as NIPT. The procedure involves drawing blood samples, which also include fetal DNA fragments. Healthcare professionals can learn more about a fetus's genetic composition by examining its DNA, which is the building block of all genes and chromosomes. A lab receives the blood sample and examines it for particular congenital conditions. Not every chromosomal or genetic disorder can be screened for by NIPT.
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