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NIPT test for Fetal Trisomy 13, 18, 21 and Other Chromosomal Aneuploidy

Non-Invasive Prenatal Testing (NIPT), also referred to as cell-free DNA screening, assesses the risk of certain genetic abnormalities in a fetus by analyzing a sample of the mother's blood. This test looks for specific trisomies (conditions in which there is an extra chromosome) as well as other types of chromosomal aneuploidy (abnormal number of chromosomes). The primary focus of NIPT centers on detecting Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), and Trisomy 13 (Patau syndrome), which are the most common trisomies that persist beyond birth. Yet, NIPT can also identify other less common chromosomal abnormalities.

  • Test NameNIPT test for Fetal Trisomy 13, 18, 21 and Other Chromosomal Aneuploidy
  • Sample TypeBlood
  • Preparations RequiredNo special preparation is needed for this test. Continue your usual diet, drinking, and medication unless instructed otherwise by your healthcare provider.
  • Report Time10 days

Upon conducting the NIPT blood test and analyzing the mother's blood sample, healthcare providers receive a comprehensive NIPT test report outlining the presence or absence of these genetic irregularities in the fetus. The processing time for NIPT test results varies, typically taking several weeks based on the specific testing facility's workload and procedures. Visit Sprint Diagnostics at your nearest locations in Hyderabad for affordable pricing and precise testing.

Home Sample Collection Process

1
Book your convenient slot
Book your convenient slot
2
Sample Collection by Phlebotomist
Sample Collection by Phlebotomist
3
Reporting of the sample at lab
Reporting of the sample at lab
4
Download Reports
Download Reports
Frequently Asked Questions

NIPT test utilizes the blood of a pregnant individual to identify congenital abnormalities in the DNA of the fetus. This examination focuses on genetic conditions, including Down syndrome, but these tests do not provide a definitive diagnosis. Instead, they provide an indication of the likelihood of a particular condition.

The NIPT blood test is a non-invasive procedure that poses no risk to either the pregnant person or their unborn child. It is a simple test that can be taken by any pregnant woman who is at least 10 weeks pregnant.

Yes, the gender of the fetus can be determined through the NIPT test by analyzing the cell-free DNA present in the mother's blood. This test is highly reliable in identifying the sex chromosomes, thus enabling early and accurate gender determination during pregnancy.

The NIPT test is a crucial tool for expectant mothers as it evaluates the likelihood of specific genetic irregularities in the unborn child, providing timely identification of disorders such as Down syndrome. This enables parents to make informed choices regarding possible interventions or preparartion for the child's needs.

NIPT results are highly accurate for common chromosomal abnormalities but not 100% accurate. Confirmatory tests may be required to account for the potential occurrence of false positive or negative results.

A positive NIPT outcome indicates an increased likelihood of specific genetic conditions. It is advisable to undergo additional diagnostic examinations, counseling and discussions with healthcare experts to gain further clarity and make informed decisions.

The price of NIPT blood test in ₹15000. Make an appointment with Sprint Diagnostics at a your nearby locations.

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