What is NIPTunegx® (Non-Invasive Prenatal Testing)
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Why NIPTunegx®
A non-invasive and safe DNA-based blood test that can be performed in your early pregnancy stages to estimate the risk of your baby being born with a genetic abnormality, such as Down syndrome.
Whole genome screening
10ml blood sample
High Sensitivity
Incorporates prior risk using First Trimester Combined Test
Individualized reports
Rapid turnaround time
Optional genetic counselling
Optional fetal sex identification, as per Local Government Regulations
Is NIPTunegx® for you
Highly recommended
Advanced maternal age (>35 years)
Advanced paternal age (>40 years)
Ultrasound abnormalities e.g., shortened long bones
Family history of genetic disorders
Suitable
Singleton or twin pregnancies
IVF pregnancy
Unsuitable
Received an organ transplant
Has or had cancer
Carries a chromosomal imbalance
Had a transfusion of heterologous cells in the last year
Has a complete or partial monosomy X (Turner syndrome)
How NIPTunegx® works
