Request appointment

It’s recommended to get checked if:

You want early, accurate information about your baby's chromosomal health.

You or your partner have a family history of genetic conditions.

You want to know your baby's sex and other genetic traits before birth.

You've experienced a previous pregnancy loss and want genetic insights.

You are planning a pregnancy and want to assess genetic risks.

You want reassurance and peace of mind during pregnancy.

Tests

Non-Invasive Prenatal Test FAQ`s

NIPT (Non-Invasive Prenatal Test) is a safe, non-invasive test that analyzes fetal DNA from the mother’s blood. It helps detect chromosomal conditions like Down syndrome, Edwards syndrome, and Patau syndrome, and can also reveal the baby’s sex and certain genetic traits.
The test screens for trisomies 13, 18, and 21, sex chromosome abnormalities, 22q11.2 deletion syndrome, and in some packages checks whether the mother is a carrier for genetic disorders such as cystic fibrosis or spinal muscular atrophy.
A simple blood sample is taken from the mother’s arm. The procedure is safe, painless, and poses no risk to the baby.
It is recommended after the 10th week of pregnancy, when there is enough fetal cell-free DNA in the bloodstream for accurate analysis.
Results are typically ready in 5–15 days, depending on the specific NIPT package chosen.
Results provide important information for understanding your baby’s genetic health, planning your pregnancy, and making informed decisions with your healthcare provider. They give parents peace of mind and guidance for early interventions if needed.
Yes, NIPT is non-invasive and does not involve risk to the fetus, unlike traditional invasive procedures such as amniocentesis.
Yes, some comprehensive NIPT panels combine aneuploidy screening with carrier testing to assess both fetal and maternal genetic risks.