Non-Invasive Prenatal screening Test is an innovative genetic test for pregnant women at risk of foetal Down syndrome (trisomy 21), Edwards’ syndrome (trisomy 18), and Patau syndrome (trisomy 13).
Now, this test also makes it possible to screen for other rarer chromosome abnormalities: autosomal abnormalities, deletions and duplications greater than 7 megabases.
It can be performed with a single blood sample obtained from 10 weeks (gestational age), which is equivalent to being eight weeks pregnant.
As a French laboratory and European leader in specialised medical pathology testing, Eurofins Biomnis has been an expert in the new generation of DNA sequencing techniques for many years and has acquired extensive know-how in the areas of prenatal genetics and biology.
Experts in their fields, the qualified prenatal diagnostics biologists responsible for Ninalia NIPT at Eurofins Biomnis support prescribers, Laboratories and their patients in the implementation of this innovative genetic test.
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