NACE is a non-invasive prenatal test. This means that it is completely safe for you and your baby: a small blood sample, just like in any other routine blood analysis, is sufficient to perform the test. NACE uses the latest sequencing technology to analyse fetal DNA to detect the most common anomalies with high precision and reliability.
NACE® detects abnormalities in chromosomes 21, 18, 13 and the most common anomalies in the sex chromosomes (X and Y).
NACE 24 Extended analyzes all 24 chromosomes and identifies microdeletions associated with 6 major genetic syndromes.
T21: Down Syndrome; T18: Edwards Syndrome; T13: Patau Syndrome; 45, X: Turner Syndrome
NACE is available to all pregnant women from week 10 of pregnancy.
This test is recommended if:
(Preimplantation Genetic Testing for Monogenic disorders)
PGT-M helps couples with a risk of transmitting a genetic disease. This genetic test Prevents the transmission of inherited disorders to future children and achieve a healthy pregnancy.
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ERA® is the first diagnostic test that determines each woman's unique personalized embryo transfer timing, therefore synchronizing the embryo transfer with the individualized window of implantation. Indicated for patients who have experienced repeated implantation failures.
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Genetic disorders can’t be cured, but they can be prevented.
CGT is an important genetic test when planning a family, because it helps to determine the risk of having a child with a genetic disease.
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