Approximately 1% of All Babies Will Be Born With a Chromosomal Abnormality
Fetal chromosomal abnormalities are causing physical disability and/or mental retardation 70% of syndromic congenital abnormalities are contributed by Trisomy T21, T18 or T13 and 10% by Turner syndrome (Monosomy X)
The risk of trisomy increases significantly with maternal age
The choice of the appropriate testing strategy and a quick response are key factors to minimize the stress.
This is why we offer a turnaround time of seven business days for most prenatal analyses (known variants, deletion/duplication analysis, single gene sequencing) and of less than 15 business days for NGS (next generation sequencing) analyses.
In addition, our medical experts are always available for your support before, during and after the analysis.
We offer genetic, non-invasive prenatal testing (NIPT) to screen for the most common fetal chromosomal abnormalities. Our test combines the latest next generation sequencing technology with expert medical reporting.
Starting Material
- Chorionic villi
- Amniotic fluid
- Fetal DNA
- Cord blood (for late pregnancies) as possible material
You have the option to send us tubes with already cultivated cells. Alternatively, we offer our cell cultivation service.
Why choose NoorDx?
Rapid
Delivering results in days
Innovative
Pioneering solutions in genomics testing to save lives
Confidential
Providing the highest levels of patient privacy and advanced data security
World-class
Granting access to a team of expert genetics within our state-of-the-art lab