Everything you need to know about your NIPT test report

The NIPT test report will provide comprehensive information on the risk factor for developing a chromosomal or genetic condition. The screening test can measure for Down syndrome, Edwards syndrome, Patau syndrome, Turner syndrome, and other developmental conditions.

The results of the test can help you know if you need to make special preparations for the baby. The test requires a sample of the blood from the mother without harming the fetus, making it a vital screening examination during the 11-17 week gestational period.

Essentially, the NIPT test measures the levels of cfDNA (cell free DNA) in the blood from the placenta. The fragments of DNA from the foetus are present in the mother's blood which can be used for testing and analysis.

It is important to note that the NIPT test report will provide the likelihood of the presence of a chromosomal condition. It can't specifically tell you whether your baby has a chromosomal condition.

The screening exam is a preliminary test, after which further testing must be performed for more accurate results. The positive predictive value is generated via the test, which can help in understanding the risk factor present.

Screening tests, such as NIPT, are vital to know if your baby is at risk of developing a chromosomal condition. In the 10-12 week period of your pregnancy, you should get the non invasive prenatal testing NIPT done for testing whether a genetic condition is present.

NIPT is a critical test to have performed as it's important to know what the potential risk factors can be. The NIPT results will indicate with clarity a risk potential for a range of chromosomal conditions. You can take the right measures after the NIPT is done to provide proper care for your child after delivery.

The following tests should be covered in the NIPT test report.

It is one of the most common conditions, in which the abnormal cell division creates additional genetic material from chromosome 21.

Children may have slow growth before birth and lower birth weight with Trisomy 18.

It is a developmental condition associated with ID (intellectual disability) and physical abnormalities.

It is a condition in which 1 of the X chromosomes is partly present or completely missing.

It is a condition in which a male child is born with an extra copy of the X chromosome.

In this condition, an extra X chromosome in present in some female babies.

It is a rare condition in which the body child receives an additional Y chromosome from the father.

The blood sample is drawn in a small tube, after which it is sent to the laboratory for further testing. The tests for the various chromosomal conditions are performed giving you a complete report.

You can book the NIPT test in India through MyDiagnostics.

The price of the complete NIPT test in India with at home convenience is INR 12500.

You can get the NIPT test report within 15 days of testing.

The NIPT test is highly recommended during the 11 to 17 week period of pregnancy.

Basic documents such as your prescription, USG, dual & quadruple marker report, and photo ID are required for the NIPT testing procedure.

 *Medical Disclaimer - The following information is for educational purposes only. No information provided on this website, including text, graphic, and images, are intended as substitutes for professional medical advice. Please consult with your doctor about specific medical advice pertaining to your condition(s).