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NIPT (Non Invasive Prenatal Testing)

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NIPT is a safe and effective method for screening your unborn baby for chromosomal anomalies. Includes Trisomy 13, 18, 21 and Down's syndrome, XO, XXY, XYY and XXX

This is a first-line test globally recommended for detecting fetal abnormalities and eliminates the need for invasive methods like amniocentosis/chorionic villus sampling.

Recommended for: High-risk pregnancies, family history of aneuploidy, advanced maternal age, abnormal ultrasound.

Sample type: 9-10 ml maternal blood in cell-free DNA BCT Streck tube, at minimum 10 weeks of gestation.

Product features: Accuracy of 99% Fast TAT of 15 days Includes all trisomies and 23 pairs of chromosomes (whole fetal genome)

More Information
Gender Female
Age 16-20, 21-30, 31-40, 41-50
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