Prenatal screening test offers several benefits, including high accuracy in detecting common chromosomal abnormalities. It is a non-invasive procedure that only requires a blood draw from the mother, allowing for early detection as early as 10 weeks into pregnancy.
Results in 10-15 days
NIPT is most often used to look for chromosomal disorders that are caused by presence of an extra or missing copy (aneuploidy) of chromosome. The test will screen for different types of chromosomal abnormalities. It includes 22 chromosomes, Trisomy 21 (Down Syndrome), Trisomy 18 (Edwards' Syndrome) and Trisomy 13 (Patau Syndrome)