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Ninalia NIPT The prenatal trisomy screening test based on maternal blood sample

Non-Invasive Prenatal Testing for trisomies 13, 18 and 21

Non-Invasive Prenatal screening Test is an innovative genetic test for pregnant women at risk of foetal Patau syndrome (trisomy 13), Edwards’ syndrome (trisomy 18) or Down syndrome (trisomy 21).

It can be performed with a single blood sample obtained from 10 weeks (gestational age) which is equivalent to being 8 weeks pregnant.

Rapid, reliable and safe, NIPT is a screening option that enables detection of trisomies 13, 18 and 21 while limiting the required number of invasive tests (amniocentesis…).

How does it work?

Besides maternal DNA, the blood of pregnant women contains foetal DNA originating from the placenta.

The identification of this foetal DNA in the maternal blood, combined with the development of a new technology (Next Generation Sequencing) capable of counting all genetic material sequences in a maternal blood sample, makes it possible to determine whether a trisomy is present in the foetus.

Advantages of Ninalia NIPT

99 % Detection rateof Ninalia NIPT 1 Single blood sample 10 Available from 10 weeks (gestational age) 5 Results availablewithin 5 business days 95 % Can minimize unnecessary invasive sampling by 95%

Find your nearest testing centre As Ninalia NIPT requires a specific sample tube, don’t forget to make an appointment in advance with your local laboratory for specimen collection.

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