No. 1 NIPT test in the world
A Mirror of Your Baby
- Non-invasive prenatal screening test to detect the risk of chromosomal abnormalities in fetal development during pregnancy.
have been conducted
According to WHO
3000-5000 Children
Born with Down syndrome worldwide each year
Did you know?
NIFTY®
Introducing the concept of safe and reliable non-invasive prenatal Screening Test.
Consult with your doctor to get the latest information on the benefits of NIFTY® for you and your future little one.
Begin Your Prenatal PlanningWomen in their 10th to 24th week of pregnancy
Age 35 and above
Contraindications for invasive prenatal testing
Family history and previous pregnancies with chromosomal abnormalities
Ultrasonography findings indicating increased risk for chromosomal abnormalities
History of miscarriage
Pregnant women who have undergone in vitro fertilization (IVF)
Need for certainty after previous screening results
Who might benefit from NIFTY®?
Why choose NIFTY®?
Safe & Reliable
Non-invasive with no risk of miscarriage. Over 14.3 million NIFTY® tests have been conducted to date with the fastest TAT.
Accurate
Proven sensitivity and specificity >99% based on research involving nearly 147,000 pregnancies.
Comprehensive
Screens all 23 pairs of chromosomes for ≥92 genetic conditions.
Insured*
Provides insurance coverage in cases of false negatives or false negatives up to Rp. 800 Million.
Coverage by NIFTY® Insurance
High-Risk Result
You will receive coverage up to approximately Rp. 9 million for confirmatory test (such as amniocentesis, CVS, PUBS, etc.)
False Negative Result
You will receive coverage approximately between Rp. 40 to million and Rp. 800 million.*
FAQ
NIFTY® is a non-invasive prenatal test (NIPT) that is safe, simple, and highly accurate in detecting the risk of certain genetic conditions, providing a much more accurate risk indication compared to conventional screening procedures. Over 14,3+ million tests have been conducted worldwide, making it one of the most comprehensive NIPT tests available.
Trisomy is a genetic condition where an individual has an extra chromosome in a pair of chromosomes.
An example is Down syndrome, where individuals have three copies of chromosome 21 instead of the usual two. This can lead to various health and developmental issues in affected individuals.
In simpler terms, we can imagine that in each of our body cells, we have a genetic instruction book called chromosomes. Trisomy occurs when that instruction book has an extra page, which can cause various problems in the body.
1. Trisomy 21 (Down syndrome)
2. Trisomy 18 (Patau syndrome)
3. Trisomy 13 (Edwards syndrome)
4. Rare Autosomal Aneuploidies (such as Trisomy 9, Trisomy 16, Trisomy 22)
5. Microdeletion/microduplication syndromes (≥92 types)
6. Sex Chromosomal Aneuploidies (such as XO, XXY, XXX, XYY)
7. Incidental findings
8. Other aneuploidies
9. Fetal gender
NIFTY® requires the collection of 6-10mL of maternal blood to analyze fetal cell-free DNA, where during pregnancy, the baby’s DNA will circulate into the mother’s bloodstream.
Yes, we provide insurance coverage for your NIFTY® results, under the following conditions:
High-Risk Results
- If you receive High-Risk Results, if one or more of your NIFTY screening results are high-risk, the cost of further confirmatory diagnostic tests will be covered up to approximately 9 million rupiah.
False Negative Results
- Low-Risk Result A if one or more of your NIFTY screening results are low-risk and you are declared high-risk during further confirmatory diagnostic tests, you will receive coverage up to approximately 40 million rupiah.
- Low-Risk Result B if one or more of your NIFTY screening results are low-risk and you do not undergo further confirmatory diagnostic tests, but the baby is born with a genetic disorder, you will receive coverage up to approximately 800 million rupiah.