OUR SERVICES
INDIVIDUALS
Novo NIPT
Taking care of your baby while you are pregnant is extremely important
This test is designed to assess the likelihood of your baby developing certain genetic conditions during his or her lifetime. Novo NIPT is an accurate and safe screening test used to determine if your baby has a low or high chance of developing certain genetic conditions.
NIPT Basic
- Common trisomies
- -Down syndrome (Trisomy 21)
- -Edwards syndrome (Trisomy 18)
- -Patau syndrome (Trisomy 13)
- Sex Chromosome Aneuploidies
- -Turner syndrome (45,X) -Klinefelter syndrome (XXY)
- -Triple-X (XXX)
- -XYY Karyotype
NIPT Plus
- Common trisomies
- -Down syndrome (Trisomy 21)
- -Edwards syndrome (Trisomy 18)
- -Patau syndrome (Trisomy 13)
- Sex Chromosome Aneuploidies
- -Turner syndrome (45,X)
- -Klinefelter syndrome (XXY)
- -Triple-X (XXX)
- -XYY Karyotype
- Rare trisomies
- Microdeletion/Microduplication syndromes
- Large segment deletion/duplication syndromes (>10MB)
Novo-NIPT Advantages
SAFE
Non-invasive with
no risk of
miscarriage
ACCURATE
Proven 99.5%
sensitivity for
detection of trisomy
conditions
SIMPLE
Test from a small
10ml maternal
blood sample
RAPID
Results available
from 7 - 14
working days
Why is this test right
for me and my
baby?
non-invasive prenatal testing (NIPT) is recommended for all pregnant women.
- Advanced maternal age > 35 years.
- Positive maternal serum screening test.
- Abnormal fetal ultrasound results.
- A previous history of having an affected pregnancy.
- Positive family history of chromosomal abnormalities, such as Down Syndrome.
This test can be performed after 10 weeks of pregnancy.
A simple blood test from the mother, no need to worry.
Ask your healthcare provider or contact Novo Genomics for more information
Novo’s lab team
generate results
you
can trust
Our MOH certified laboratory uses
next-generation sequencing, advanced liquid-handling
robots, and customized software to ensure the integrity of our
results
