No. 1 NIPT Test in the World
That are crucial to detect early for optimal fetal development during pregnancy period
Born with down syndrome worldwide each year
Consult with your doctor to get the latest information on the benefits of NIFTY® for you and your future little one.
Women 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
Non-invasive with no risk of miscarriage. Over 14.8 million NIFTY® tests have been conducted to date with the fastest TAT
Proven sensitivity and specificity >99% based on research involving nearly 147,000 pregnancies
Screens all 23 pairs of chromosomes for ≥92 genetic conditions
Provides protection coverage for false negatives of up to Rp. 800 million.
You will receive coverage up to approximately Rp. 9 million for confirmatory test (such as amniocentesis, CVS, PUBS, etc.)
You will receive coverage ranging from approximately Rp. 40 million to Rp. 800 million.
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 14,8+ 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 protection coverage for your NIFTY® results, under the following conditions:
High-Risk Results
False Negative Results
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