NIPT
- Delivers 99.9% of High Accuracy
- TAT - 7 to 10 working days
NIPT is an easy, secure, and non-invasive prenatal screening that offers expectant parents reliable genetic insights about their unborn child. This test employs sophisticated bioinformatics techniques to analyse fetal DNA (originating from the placenta) found in the mother's blood, for detecting genetic abnormalities.
Prevalence
Conditions that NIPT can detect
NIPT can identify prevalent aneuploidies in all 23 pairs of chromosomes including sex chromosome aneuploidies and rare autosomal aneuploidies.
NIPT Basic
- Chromosome 13 ∼ (Patau syndrome)
- Chromosome 18 (Edward's syndrome)
- Chromosome 21 *(Down syndrome)
- XXY (Klinefelter syndrome)
- XYY (Jacobs Syndrome)
- XO (Turner syndrome)
Screens for chromosomal aneuploidies in
NIPT with Microdeletion
- DiGeorge(22q11.2)
- Angelman (15q11.2)
- Prader-willi(15q11.2)
- Cri-du-chat(5p)
- Wolf-Hirschhorn syndrome(4p)
- 1p36 deletion
Screens for chromosomal aneuploidies in all the 23 Chromosomes Microdeletions
NIPT All chromosome
Screens for chromosomal aneuploidies in all 23 pairs of chromosomes.
NIPT Twins
NIPT Twin : Screens for all 23 pairs of chromosomes in both the fetus
NIPT does not test for the gender of the fetus. Setgene is a PC & PNDT certified company
Key Highlights
A detailed analysis of the fetal genetic makeup
Improved Testing Efficacy
Low Test Failure Rates
Quickest Delivery of Test Results
Why is it important to have the NIPT test?
- Helps identify fetuses at risk of serious chromosomal abnormality
- Offers reassurance to expectant parents.
- Facilitates improved care for a child's genetic health by delivering early insights.
- Prepares for the birth and early intervention wherever possible
At what stage of pregnancy can the NIPT test be performed?
- The NIPT screening test can be performed from as early as 10 weeks of pregnancy.
Indications to offer NIPT
- All pregnant women, regardless of age, have the option to undergo prenatal testing, who wish to get more information about their baby.
- Advanced maternal age (>35 years)
- Abnormal ultrasound findings
- Family history or a previous child with a chromosomal aneuploidy like Down syndrome
- Couple with history of recurrent pregnancy loss
- In case of high risk serum screening results
How is Setgene NIPT better?
- High sensitivity and specificity for reported results
- Low false positive rates.
- Accuracy of 99.9%
- Pre and post-test genetic Counselling for all patients.
- TAT - 7 to 10 working days
