NIPT - Non-Invasive Prenatal Screening 23+ (ADVANCED)

Prenatal Genetic Screening at Home

Early, Accurate Insights for a Confident Pregnancy

The advanced Prenatal screening offers a highly accurate, non-invasive way to screen for genetic conditions early in pregnancy. A simple blood test provides crucial insights without risk to you or your baby. Conducted from the comfort of your home, this test delivers reliable results, helping you make informed decisions with confidence. Early detection for a healthier future. Understanding genetic risks can provide peace of mind throughout your pregnancy. Reliable screening supports better planning and preparation for your baby’s health. Stay informed with a safe and convenient prenatal testing option.

Test Includes :

Comprehensive test package for a detailed insight into your health status.

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FAQ's

What is the NIPT 23 + (ADVANCED) test?

The NIPT 23 + (ADVANCED) test is a non-invasive prenatal screening that analyzes fetal DNA from a simple blood sample taken from the mother. This test screens for genetic conditions such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), Patau syndrome (Trisomy 13), sex chromosome abnormalities, and microdeletions.

The test works by detecting fetal DNA in the mother’s blood, which can provide valuable information about the baby’s genetic health. The test is non-invasive, meaning there are no risks to the baby, unlike traditional invasive procedures like amniocentesis or CVS.

This advanced test screens for three trisomies (21, 18, and 13), sex chromosome abnormalities (such as Turner syndrome or Klinefelter syndrome), and microdeletions, which are small genetic changes that can cause serious disorders like DiGeorge syndrome.

You can take the NIPT 23 + (ADVANCED) test as early as 10 weeks into your pregnancy. This makes it one of the earliest and most accurate genetic screenings available for expecting mothers.

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