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NIPT Test at Home

Non-invasive Prenatal Test (NIPT)

Accurate & Affordable Prenatal Screening For A Healthy Pregnancy

Non-invasive prenatal testing (NIPT) is a highly accurate screening method used during early stages of pregnancy to detect genetic conditions in the developing baby. It analyzes fetal DNA present in the mother’s blood and identify conditions such as Down syndrome and Patau syndrome. This test provides valuable information during the developing stages of the fetus, allowing expecting parents and healthcare providers to make informed decisions about the health of their baby. NIPT is a safe procedure for both mother and baby and offers a non-invasive alternative to traditional diagnostic tests.

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Most Affordable NIPT Screening In Dubai - Starting From Just AED 99 Only

Check your baby’s health with comprehensive screening for chromosomal abnormalities in early stages of pregnancy.

Standard NIPT

Screens for common abnormalities such as Down syndrome, Edwards syndrome and Patau syndrome, providing a highly accurate picture of fetus health as early as 10th week of pregnancy.

Expanded NIPT

In addition to standard screening, this test includes a broader range of chromosomal conditions and microdeletions, providing information on genetic abnormalities in the early stages.

Gender Determination

Learn about the sex of your baby as early as 10th week of pregnancy. Gender determination can be combined with standard or expanded NIPT providing additional information.

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Sample Collection

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Results

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Fast & Accurate Lab Testing

NIPT – An Essential Tool To Check Your Baby’s Genetic Health

NIPT is crucial for early detection of many genetic conditions that may affect your baby’s physical and mental health. Early diagnosis allows for better planning and preparation, ensuring appropriate medical care and support are in place if needed. NIPT also gives you reassurance and peace of mind that your baby’s health is good.

NIPT is particularly beneficial for:

  • Pregnancies happening after the age of 35.
  • When you are at risk of genetic abnormalities.
  • When you have a family history of chromosomal abnormalities.

Identifying potential issues early can benefit parents to make informed decisions about their pregnancy and receive timely interventions, thus improving outcomes for both mother and baby.

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Frequently Asked Questions

NIPT (Non-Invasive Prenatal Testing) is a screening method that analyzes fetal DNA in the mother’s blood to detect certain genetic conditions in the developing baby. A blood sample is taken from the mother, which is then analyzed in a laboratory to detect fetal DNA and identify any genetic abnormalities. The test is typically performed around the 10th week of pregnancy.

NIPT can detect common chromosomal abnormalities such as Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13). Expanded NIPT can screen for additional genetic conditions and microdeletions.

Results are typically available within 7 to 10 days. Your healthcare provider will discuss the findings with you and provide guidance on the next steps if any abnormalities are detected.

Yes, NIPT can determine the baby’s gender as early as the 10th week of pregnancy. This information can be included in the test results if desired.

NIPT is highly accurate but it is not a diagnostic test. It is a screening method that provides information about the risk of genetic conditions. Further testing is needed to confirm any positive results.