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:
<li class="bullet-checkmark" You are at high risk of chromosomal alterations after your first trimester screening
<li class="bullet-checkmark" You have a previous history of births with chromosomal abnormalities
Avoid implantation failure by establishing the best day and time for embryo transfer
More information
Carrier Genetic Test
Determines the risk of having a child with a
genetic disease
