Natris™ Plus-Responsibly Expanding the Accurate, Reliable, and Relevant Natris™
The Natris™ Plus for singleton pregnancies screens for Down syndrome, Trisomy 18, Trisomy 13 and additional options that you and your healthcare provider may choose to select, as shown below:
- Select microdeletions such as 1p36 deletion, 4p- (Wolf-Hirschhorn syndrome), 5p- (cri-du-chat syndrome), 15q11.2 (Prader-Willi syndrome/Angelman syndrome), and 22q11.2 deletion (DiGeorge syndrome)
- Sex chromosome aneuploidies (monosomy X, XXX, XXY, and XYY) are included if requested; fetal sex (XX or XY) will be reported if no sex chromosome aneuploidy is detected.
- Aneuploidy (trisomy) of all chromosomes, including sex chromosome aneuploidies.
How It Works
A sample of your blood is drawn and the genetic material (DNA) from your baby is tested. Natris™ takes a deeper approach to the science, using an advanced technology called “Whole Genome Sequencing” to analyze millions of DNA fragments per sample and accurately count the number of chromosomes present.
MX (Turner Syndrome)
XX (female fetus)
XY (male fetus)
Turn around time: Results can be expected 5-8 business days from the time the sample is received at the laboratory.
Learn more about why Eurofins NTD Genetics has been the laboratory to trust for over 30 years.Learn More
Our Goal is to Educate and Empower
Know your choices, understand your options, and talk you your healthcare provider about the best prenatal screening program for you.Learn More