NIPT Test (Non-Invasive Prenatal Testing)

• High Accuracy: Our NIPT test delivers unparalleled accuracy of 99.9%, giving you peace of mind.

• Safety: Non-invasive and risk-free for both the baby and the mother.

• Comprehensive Screening: Detects a wide range of genetic variations and disorders.

• Assurance: Provides expectant parents with detailed genetic information for informed decision-making.

• Comprehensive Fetal Genome Screening:

  • Screens the entire fetal genome, not just trisomies in chromosomes 21, 18, and 13.

• Enhanced Test Performance:

  • Sensitivity and specificity of >99.9% for Trisomy 21, 18, 13.

• Low Test Failure Rates:

  • NIPT offers a >99% call rate, minimizing test failure rates.

• Fastest Test Results:

  • The NIPT features a fast three-step automated workflow for NIPT.

  • Turnaround time is less than or equal to 7 working days, providing quick results.

• Carrier Screening: Identify carriers of specific genetic conditions.

• Rhesus D Track: Monitor Rhesus D status during pregnancy.

• PGT-A, M, S: Preimplantation Genetic Testing for Aneuploidies, Monogenic disorders, and Structural rearrangements.

• Recurrent Pregnancy Loss Test: Evaluate potential genetic factors contributing to recurrent pregnancy loss.

• Molecular Cytogenetic: Analyze chromosomal abnormalities.

• Maternal Serum Screening: Screen for certain conditions using maternal serum markers.

1. Identifies Fetuses at Risk of Serious Chromosomal Abnormality:

   • The NIPT test helps detect potential serious chromosomal abnormalities in the fetus, providing crucial information for informed decision-making.

2. Provides Reassurance to Expecting Parents:

   • Expecting parents can gain peace of mind knowing the genetic health status of their baby, reducing anxiety and uncertainty during pregnancy.

3. Enables Better Management of Child’s Genetic Health:

   • Early detection through NIPT allows for better management of a child’s genetic health by providing early information for necessary interventions or preparations.

4. Facilitates Early Intervention and Preparation for Birth:

   • NIPT results enable healthcare professionals to prepare for the birth and plan early interventions whenever possible, optimizing the baby’s health outcomes.

1. The NIPT screening test can be performed as early as 10 weeks of pregnancy, providing early insights into the baby’s genetic health.

NIPT is recommended for all pregnant women seeking insights into their baby’s development, irrespective of their age or risk factors. Medical societies advocate NIPT as the primary screening method for all pregnancies, regardless of risk. Physicians may particularly recommend this test for pregnancies where:

• The woman is above 30 years of age.

• High risk for abnormality is identified through serum screening.

• Certain abnormalities are detected on ultrasound.

• There is a family history of chromosomal conditions or birth defects.

• Couples have previously had a child with a chromosomal disorder.

• A couple has a history of infertility or pregnancy loss (miscarriages or stillbirths).

NIPT is capable of detecting various chromosomal abnormalities, including:

• Trisomy 21 (Down Syndrome)

• Trisomy 18 (Edwards’ Syndrome)

• Trisomy 13 (Patau Syndrome)

• Turner Syndrome (Monosomy X/XO)

• Klinefelter Syndrome (XXY)

• Triple X (XXX)

• Jacob’s Syndrome (XYY)

Our NIPT test is also available for twin pregnancies, offering comprehensive screening for:

• Trisomy 21

• Trisomy 18

• Trisomy 13