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Trichy Fetal Medicine and Fertility Centre
Screening and tests

Can NIPT Detect Down Syndrome?

NIPT is a blood test that screens for Down syndrome from about 10 weeks of pregnancy. Learn what it can and cannot tell you, and what happens next.

In this guide
Pregnant woman having a routine blood sample taken in a bright clinic

How NIPT works

During pregnancy, tiny fragments of the baby's DNA circulate in the mother's blood. NIPT reads these fragments and checks whether there is an extra copy of chromosome 21, which causes Down syndrome. It can also look at chromosomes 18 and 13, and sometimes the sex chromosomes.

Because only a blood sample from the mother is needed, there is no risk to the baby from the test itself.

What NIPT can tell you

  • Whether the chance of Down syndrome is low or high.
  • The chance of trisomy 18 and trisomy 13 on most panels.
  • The baby's sex, if you choose to know.

What NIPT cannot tell you

  • It cannot confirm Down syndrome. It only estimates the chance.
  • It does not check for every genetic or structural condition.
  • It does not replace the detailed anomaly scan.
  • Rarely, the result can be unclear or fail, and the test may need to be repeated.

Who should consider NIPT

NIPT can be offered to any pregnant woman. It is especially useful when:

  • The first trimester screening shows an increased risk.
  • The mother is of higher age.
  • There has been a previous pregnancy with a chromosomal condition.
  • A scan has shown a soft marker.

What happens after the result

A low-risk result is reassuring, but the routine scans should still be done. A high-risk result does not mean the baby definitely has Down syndrome. Your doctor will usually advise a diagnostic test such as amniocentesis or CVS, along with counselling, so you can take decisions with full information.

If you remember one thing

Choosing a prenatal test can feel overwhelming. Dr Malathi G. Prasad at Trichy Fetal Medicine and Fertility Centre in Trichy can explain which test suits your pregnancy and help you understand the results in plain language.

When you are ready, the NIPT service page covers timings and preparation; questions about your own situation are best put to our specialists.

Common questions

Sources

  1. Society for Maternal-Fetal Medicine. SMFM Consult Series 74: cell-free DNA screening. · publications.smfm.org
  2. NHS. Screening for Down's syndrome, Edwards' syndrome and Patau's syndrome. · nhs.uk

This guide is for general information and does not replace a consultation with a fetal medicine specialist.

In line with the PCPNDT Act, we do not perform or support sex determination.

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NIPT

A simple blood test from the mother that screens for common chromosomal conditions, with no risk to the baby.
About NIPT

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