Down syndrome - Fetal DNA test | Ninalia NIPT

NIPT by Biomnis The new prenatal trisomy screening test based on maternal blood sample

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high risk pregnancy

Biomnis: A European Leader in Non-Invasive Genetic Screening Tests

Eurofins Biomnis is a European leader in the sector of specialized medical pathology, offering a large range of innovative genetic screening tests. The group has developed non-invasive testing kits that deliver fast and remarkably accurate results, detecting pathologies and disorders such as Down Syndrome, Patau Syndrome and Edwards' Syndrome through fetal and maternal cell-free DNA sampling.  Through a NIPT test, it can be determined whether the risk of fetal defects is high or low, reducing invasive procedures by up to 95%.

Prescribing a non-invasive prenatal screening method for the detection of common trisomies and fetal anomalies offers reliable initial risk assessment for common abnormalities. With detection rates exceeding 99%, NIPT screening is generally recommended for mothers with risks greater than 1 in 1,000 according to serum markers. A positive result indicates a strong suspicion that anomalies relating to one or more genetic conditions are present. Available starting at 10 weeks of pregnancy, the test provides remarkably accurate screening from the first trimester of pregnancy. Eurofins Biomnis follows the international recommendations of the American College of Obstetricians and Gynecologists (ACOG) and the Society for Maternal-Fetal Medicine (SMFM).

Advantages of NIPT by Biomnis

> 99 % Detection rateof NIPT test 1 Single blood sample 10 Available from week 10of amenorrhoea 7 Results availablewithin 7 working days 95 % Can minimize unnecessary invasive sampling by 95%
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