NIFTY® - Non-Invasive Fetal TrisomY test
The World’s Leading Non-Invasive Prenatal Test (NIPT)
NIFTY® (Non-Invasive Fetal TrisomY test) is a safe, simple, non-invasive prenatal test (NIPT), which offers screening for certain genetic conditions from as early as week 10 of pregnancy.
Using the latest genetic sequencing technology, NIFTY® has over >99% accuracy for the three most common trisomy conditions present at birth, which are Down Syndrome, Edwards Syndrome and Patau Syndrome.
The Advantages Of The NIFTY® Test
Trusted
Over 9.4 million tests conducted worldwide and validated on a study of over 147,000 pregnancies
Accurate
>99% sensitivity for detection of trisomy conditions such as Down syndrome.
Comprehensive
Screening across all 23 pairs of chromosomes up to 96 genetic conditions
Simple
Test from a small 10 ml maternal blood sample as early as week 10 of pregnancy
Safe
Non-invasive with no risk of miscarriage
Fast
Report delivered within 10 working days
Insured
Offering insurance in cases of false positive or false negative
Workflow
Physician orders test
Blood sample collected
Results sent to physician
NIFTY test is suitable for
Maternal age 35 years or
older at delivery
Fetal ultrasonographic findings indicating an increased risk of aneuploidy
Require reassurance following previous screening result
Contraindications for invasive prenatal testing, such as placenta prevaria, risk of miscarriage or HBV infection
History of a prior pregnancy with a trisomy
Received IVF Treatment or have previously suffered from habitual abortion
Available from week 10 of pregnancy, the NIFTY® test gives you an early option to know more about the genetic health of your baby.
Compared to traditional screening tests, the NIFTY® test offers higher accuracy and lower false positive rates. This means that less women will undergo invasive diagnostic procedures such as amniocentesis or chorionic villus sampling which carry a 1-2% risk of miscarriage.
The NIFTY® test is available to any pregnant woman from the 10th week of pregnancy but is particularly suitable for pregnant women who exhibit certain indications which are highlighted below.
Remember, non-invasive prenatal testing may or may not be right for you. Prior to undertaking any non-invasive prenatal testing, you should consult a qualified healthcare professional regarding any risks, diagnoses, treatment and/or any other potentially relevant healthcare issues. Non-invasive prenatal testing is not diagnostic, which means that is does not test with 100% accuracy.
Package Test Options
| Trisomies |
|---|
 Trisomy 21 (Down Syndrome) |
| Trisomy 18 (Edwards Symdrome) |
| Trisomy 13 (Patau Syndrome) |
| Gender Identification |
|---|
| Male / Female |
| Trisomies |
|---|
| Trisomy 9 |
| Trisomy 16 |
| Trisomy 22 |
| Other Trisomies |
| Sex Chromosome Aneuploidies |
|---|
| Monosomy X (Turner syndrome) |
| XXY (Klinefelter syndrome) |
| XXX (Triple-X) |
| XYY (Jacob’s syndrome) |
| Deletion / Duplication |
|---|
| 84 kinds of deletion / duplication |
| Trisomies |
|---|
| Trisomy 21 (Down Syndrome) |
| Trisomy 18 (Edwards Symdrome) |
| Trisomy 13 (Patau Syndrome) |
| Gender Identification |
|---|
| Male / Female |
| Trisomies |
|---|
| Trisomy 9 |
| Trisomy 16 |
| Trisomy 22 |
| Other Trisomies |
| Sex Chromosome Aneuploidies |
|---|
| Monosomy X (Turner syndrome) |
| XXY (Klinefelter syndrome) |
| XXX (Triple-X) |
| XYY (Jacob’s syndrome) |
| Trisomies |
|---|
| Trisomy 21 (Down Syndrome) |
| Trisomy 18 (Edwards Symdrome) |
| Trisomy 13 (Patau Syndrome) |
| Gender Identification |
|---|
| Male / Female |
| Sex Chromosome Aneuploidies |
|---|
| Monosomy X (Turner syndrome) |
| XXY (Klinefelter syndrome) |
| XXX (Triple-X) |
| XYY (Jacob’s syndrome) |
| Trisomies |
|---|
| Trisomy 21 (Down Syndrome) |
| Trisomy 18 (Edwards Symdrome) |
| Trisomy 13 (Patau Syndrome) |
| Y Chromosome |
|---|
