MaatriSeq (NIPS)

Precision Prenatal Care: Tailored to India’s Unique Genetic Landscape
Test Code
SLS165527
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What is MaatriSeq (NIPS)?

MaatriSeq is a Non-Invasive Prenatal Screening (NIPS) test that is a cell-free DNA-based screening method used to detect chromosomal abnormalities in the fetus during pregnancy. Unlike traditional methods with high false-positive rates, NIPS is a sensitive and non-invasive screening test that has been specifically developed for and validated on Indian samples and conditions.

MaatriSeq NIPS Advance

What does MaatriSeq screen for?

MaatriSeq screens for fetal chromosomal abnormalities such as:
  • Down syndrome
  • Edward syndrome
  • Patau syndrome
  • Aneuploidy for all 23 pairs of Chromosomes

Who is MaatriSeq for?

  • Individuals of advanced maternal age
  • Those with abnormal biochemical screening results
  • Those with abnormal ultrasound findings
  • Those with a previous pregnancy involving a chromosomal abnormality
Trisomy of Chromosome 21:Down Syndrome
Trisomy of Chromosome 18:Edwards Syndrome
Trisomy of Chromosome 13:Patau Syndrome
Anomalies of the Sex Chromosomes:XXX, XXY
All Chromosomal Aneuploidies:(22 Pairs)

Disclaimer: This test is exclusively available upon prescription by a certified clinician/clinical geneticist duly registered with PCPNDT guidelines.

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