Non-Invasive Prenatal Testing (NIPT)

A SIMPLE, ACCURACY, SAFE prenatal testing to check if your baby have Down syndrome or other common chromosomal abnormalities.

What is NIPT?

NIPT is an advanced and powerful risk assessment tool of detecting serious diseases which are caused by aneuploidy of chromosome 13, 18 and 21.

We are able to screen out if the fetus will be at high risk to have certain disease as early as 10 weeks of pregnancy using a single blood draw.

It will be more convenient and accurate than traditional serum screening. It also provides us a possibility to know the result earlier than amniotic fluid test.

What does GGA NIPT screen for?

GGA NIPT can screen chromosome aneuploidies, sex chromosome aneuploidies and common microdeletions as following:

Importance of Confirmation When NIPT is “High Risk"

While NIPT is an excellent screening test, it can only provide RISK ASSESSMENT.

If the NIPT result indicates high risk, a further confirmatory DIAGNOSTIC TEST is recommended to identify the condition of fetus.

Why Choose GGA NIPT?

With multiple certification and accreditation such as CAP, ISO 17025, GGA is making our best effort to provide a more valuable genetic test strategy to our clients. If you need more information of our NIPT, please contact us through the contact information on our web page.