Llabnetics Pakistan
Non-invasive prenatal screening helps to avoid unnecessary amniocentesis
Screens for the most common chromosomal abnormalities without risk to your child
Highest informativity rate in the market: we obtain results for 99.9% of the analyzed samples
Available from week 10 of pregnancy
Reduces unnecessary amniocentesis
NACE is a non-invasive prenatal screening test for the most frequent chromosomal abnormalities. The test is non-invasive, meaning that there is no risk to the fetus.
A simple blood draw from the mother allows free fetal DNA circulating in the maternal bloodstream to be detected via next-generation sequencing (NGS) technology and our proprietary bioinformatic analysis tool.
> NACE detects abnormalities in chromosomes 21, 18, 13 and the most common anomalies in the sexual chromosomes (X and Y).
> NACE 24 analyzes all chromosomes
> NACE 24 Extended analyzes all 24 chromosomes and identifies microdeletions associated with 6 major genetic syndromes.
> Single pregnancies
> Twin pregnancies
> Can give results with fetal fraction under 4%
> Natural conception
> IVF
> Egg donation
> Women of all ages
> Women of all ethnicities
> Women of all body mass index
> Suitable for cases of consanguinity
> Prevent the need for 98% of invasive tests in patients at risk for trisomy 21 (Down Syndrome)
> Reduces the number of miscarriages caused by amniocentesis or chorionic villus sampling (CVS)
> Can give results with fetal fraction under 4%
> NACE has the highest informativity rate in the market: we obtain results for 99.9% of the analyzed samples
> NACE Extended 24 incorporates the detection of all 24 chromosomes and identifies five microdeletions that are associated with major genetic syndromes
> More reliable than 1st trimester combined screening. The false positive rates of conventional tests, including biochemical screening, mean that 1 in every 20 women who test positive for Down syndrome will actually be carrying a healthy baby.
> Avoid a false sense of security: Of every 20 women carrying a baby with Down syndrome, 3 will test negative by biochemical screening.
Several scientific studies support the use of non-invasive prenatal testing for all pregnant women.
> An abnormal result in their first-trimester screen.
> A previous Down´s syndrome pregnancy
> A suspicious ultrasound finding.
> cfDNA screening is considered a screening test and not a diagnostic test.
> False non-invasive prenatal screening (NIPT) results: fetoplacental mosaicism, maternal chromosomal abnormalities, vanishing twin syndrome and/or errors associated with the procedures.
> Low-molecular-weight heparin can interfere with the analysis. If the patient is taking heparin during pregnancy, the recommendation is to perform the blood draw before heparin administration.