What is NIPT-COMP?

NIPT-COMP is an advanced Non-Invasive Prenatal Test that analyzes cell-free fetal DNA (cfDNA) circulating in the mother’s blood to detect genetic abnormalities in the developing baby — without any risk to mother or fetus.

When Can It Be Done?

✔️ From 10th week of pregnancy onward
✔️ Especially recommended for women who are:

• Aged 35 years or above

• With a history of chromosomal abnormalities

• IVF pregnancies

• Abnormal first trimester screening results

What Does NIPT-COMP Screen For?

✅ Aneuploidies (extra or missing chromosomes)

• Trisomy 21 (Down Syndrome)

• Trisomy 18 (Edwards Syndrome)

• Trisomy 13 (Patau Syndrome)

• Sex chromosome abnormalities (XO, XXY, etc.)

✅ Microdeletions & Rare Syndromes (depending on test package)

• DiGeorge Syndrome

• Prader-Willi / Angelman Syndrome

• Cri-du-chat Syndrome

✅ Fetal Sex (optional) – Gender detection not disclosed in India (as per law)