myPrenatal

A simple screening test that provides reliable answers about the health of a developing fetus. It only requires a small sample of the mother’s blood.

Why should you get screened?

myPrenatal is a non-invasive test that screens for the 3 most common syndromes

Down Syndrome

Down syndrome (trisomy 21) is associated with developmental and intellectual delays, ranging from mild to severe

Edwards Syndrome

Edwards syndrome (trisomy 18) is a condition that causes severe developmental delays and birth defects

Patau Syndrome

Patau syndrome (trisomy 13) is a condition that causes severe intellectual disability and physical defects.

Additional screening for the following sex chromosome conditions can be requested at no additional cost:

  • Turner syndrome (monosomy X)
  • Triple X (XXX)
  • Klinefelter syndrome (XXY)
  • Jacobs syndrome (XYY)
myPrenatal test is:
Safe

Routine, non-invasive blood draw, from the mother, requiring just one tube of blood (7–10 ml).

Accurate

Directly analyzes cell-free fetal and maternal DNA with our proprietary Safer algorithm; very low failure rate (0.1%).

Easy

Test as early as 10 weeks (gestational age). No limitations regarding ethnicity, BMI, ART or egg donor cases.

Fast

Results reported to provider 7-10 days after sample receipt. (Time to report may vary based on partner laboratory providing the test.)

What do you get?

A report with your results is provided to your physician with 3 possible outcomes

  1. No aneuploidy detected — No extra or missing chromosomes were detected
  2. Aneuploidy suspected (borderline value)
  3. Klinefelter syndrome (XXY)
  4. Aneuploidy detected — missing chromosomes were detected

Both “aneuploidy suspected (borderline value)” and “aneuploidy detected” results should be confirmed by an invasive procedure if a more definitive diagnosis is desired.

How to get started

1

Order the test

Contact the distributor at the bottom of this page

2

Collect your sample

Physician or lab personnel collect your sample

3

Sample is processed

Your sample gets processed at VeritasGenetics’ CLIA lab

4

Your report is ready

VeritasGenetics interprets your results and provides a report to your physician

Technical
information

Superior technology for informative non-invasive prenatal screening

myPrenatal uses an advanced technology called “Massively Parallel Sequencing” to analyze millions of DNA fragments per sample and accurately count the number of chromosomes present. It then uses a special Safer calculation method to determine if there are too many or too few copies of these chromosomes in your baby.

  • Superior technology — Strong clinical evidence showing across-the-genome analysis in a real-world population
  • Comprehensive analysis — Provides option of comprehensive sex chromosome analysis
  • Informative results — Helpful classification of results
  • Microdeletion and other aneuploidies option — Additional information on selected microdeletions and other aneuploidies (Trisomy 9, Trisomy 16) is also available

Contact

Phone: 1234-123-123-4

Address: XYZ Distributor Address

E-mail: 1234-123-123-4

About VeritasGenetics

VeritasGenetics is a global pioneer in disease prevention through accessible genetic information. By removing the barriers to genetic screening, Veritas empowers individuals and doctors to make informed lifestyle decisions that can lead to disease prevention and longer and healthier lives. Veritas is founded by leaders in genomics from Harvard Medical School and operates globally from its offices in the U.S., Europe and China.