Who Can Be Screened With Nifty® ?

12M+
Families worldwide
choose NIFTY®

10
Available from 10th gestational
week with 10ml maternal blood

>99%
Accuracy for detecting
Down syndrome

7-10
Report delivered within
7-10 working days

0%
Non-invasive with no
risk of miscarriage

147,000
Largest clinical validation to date
with nearly 147,000 pregnancies
Package Test Options

Trisomies |
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Gender Identification |
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Trisomies |
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Sex Chromosome Aneuploidies |
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Deletion / Duplication |
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Trisomies |
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Gender Identification |
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Trisomies |
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Sex Chromosome Aneuploidies |
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Trisomies |
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Gender Identification |
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Sex Chromosome Aneuploidies |
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Trisomies |
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Y Chromosome |
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Package Test Options



A Comparison of Detection Rates
Workflow

STEP 1
Physician orders test

STEP 2
8-10 mL blood sample collected

STEP 3
Sample shipped to BGI & analyzed

STEP 4
Results sent in 7-10 working days
Knowledge

Under 35
Did you know? Pregnant woman under 35 years are at risk for having an infant with Down syndrome. In Thailand, there are approximately 800,000 pregnant women in each year. From this number, infant with down syndrome is accounted for 800-1,000 persons. Since 2004, the Ministry of Public Health (MOPH) has recommended that pregnant women aged over 35 years must engage to the chromosome abnormalities testing in newborn, due to advance maternal age is related to higher risk in Down syndrome. However, the statistics of children with down syndrome reveals that 75-80 % are born from woman younger than 35 years.

“Trisomy” Genetic disease with no cure
The genetic information passed from parent to child. Thus, any changing of genes might be passed which cause of genetic disease in their child. Until now, these genetic diseases cannot be cured. Thus, treatment strategies are designed to improve signs and symptoms that associated with disorder Down syndrome is one of genetic disease. The major cause might not be passing on the gene but cause of other factors such as age of mother, mother’s egg abnormalities. Down syndrome is also known as Trisomy 21, because the alteration in the number or genetic structure of chromosome 21. The incidence at birth of Trisomy 21 is 1:800.
Publications
Publications |
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Zhang, H., et al. (2015). Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies. Ultrasound Obstet Gynecol, 45(5), 530-538. doi: 10.1002/uog.14792 |
Lau, T. K., el at. (2013). Non-invasive prenatal screening of fetal Down syndrome by maternal plasma DNA sequencing in twin pregnancies. The Journal of Maternal-Fetal and Neonatal Medicine 2013 Mar;26(4): 434-7 |