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NIPT BLOOD TEST FOR GENETIC DISORDER

NIPT BLOOD TEST FOR GENETIC DISORDER

Non-invasive prenatal testing (NIPT) is a blood test that screens for genetic abnormalities in a fetus. It's also known as non-invasive prenatal screening (NIPS) or cell-free DNA screening (cfDNA).

How it works

  • The cfDNA comes from the mother's cells and the placenta.

  • The DNA in placental cells is usually identical to the fetus's DNA.

  • NIPT analyzes DNA fragments in the pregnant person's blood.

  • These fragments are called cell-free DNA (cfDNA) because they are not contained within cells.

What it can detect

  • NIPT can detect Down syndrome, trisomy 13, trisomy 18, Turner syndrome, Klinefelter syndrome, and triple X syndrome.

  • It can also predict the fetus's sex.

When it can be done

  • NIPT can be done from 9 or 10 weeks pregnant until the end of the pregnancy.

Safety

  • NIPT is very safe and poses almost no risk of side effects to the mother or baby.

Cost

  • The cost of NIPT in India depends on the healthcare provider, the city, and the conditions being tested.

NIPT BLOOD TEST FOR GENETIC DISORDER DOOR STEP SAMPLE COLLECTION

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The R S Diagnostic Centre Difference: We leverage cutting edge technology to deliver precise and comprehensive diagnostic services. Our state of the art equipment and computerized systems ensure accurate analyses for informed medical decisions. Behind our technology-driven approach is a team of skilled technicians, radiologists, pathologists, and medical experts.
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