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nifty test is a simple blood test which detects Downs syndrome and other genetic syndromes without any risk to the pregnant woman or mother

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What is nifty test or nifty blood test ?[NIPT non invasive prenatal testing]

NIFTY test  is a simple blood test which detects Downs syndrome and other genetic syndromes without any risk to the fetus or mother.
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Human somatic cells each contains 23 pairs of chromosomes. Gain or loss of chromosomes in human cells will cause of fetal genetic defects. Trisomy 21 (Down’s syndrome), 18 (Edwards syndrome), and 13 (Patau syndrome) are the three most common chromosome abnormalities; which are caused by the presence of an extra copy of chromosome 21, 18, or 13 respectively.
This non-invasive fetal trisomy test provided by BGI is a safe and easy prenatal screening test for Downs syndrome and other trisomies. The test consists of a mere 10 ml blood sample from the pregnant woman at gestational week 10 to 24. From this blood sample, DNA from the baby is analyzed in order to examine the baby’s chromosomes (Trisomy 21, trisomy 18 and trisomy 13). With this information it is also possible to identify the gender of the baby.

 

NIFTY test Advantages:
Highly Accurate, Non-invasive, Risk Free and Early-test
Highly Accurate: Adopts the next-generation sequencing technology, detection rate > 99.9%.
Non-invasive: Only 10ml of maternal venous blood is required. Therefore, there is no risk of intrauterine infection and miscarriage.
Risk Free: Avoids intrauterine infection and induced miscarriage.
Early-test: Performed as early as 10 weeks of gestation. This allows early detection for a better clinical decision
When to be tested?
The NIFTY test is recommended between 10 and 24 weeks of pregnancy.
Who should be tested?
  1. Maternal age 35 years or older at delivery
  2. Has contraindications for invasive prenatal testing such as placenta prevaria,risk of misscarriage,HBV infection
  3. Fetal Ultrasonographical findings indicating an increased risk of aneuploidy
  4. History of prior pregnancy with trisomy

 

How to get tested?
Easy to be tested, easy to understand
After having consulted your local provider, it will be required that you complete the NIFTY approval form before the test procedure can be commenced. The blood sample required for the NIFTY test will be processed at the BGI laboratories. You will receive the test result at your local provider after 10 to 14 days.
The sensitivity and specificity of the NIFTY test are both over 99%. This means that the test can successfully identify over 99% of fetuses carry no trisomy (giving a low risk result) and fetuses with trisomy (giving a high risk result).
Where to order this test?
Any pregnant women can order this test for pre-test counseling…our authorized consultant will call or visit to explain in detail about test and its benefits in your local language.
procedure to order test?
You can opt for placing order  in various ways as per your convenience
1)Order online  visit www.healthchecker.in , place order or request call back  via our contact form available at website
2)Give call to our BGI authorized consultant Mr.gopal sindhe mobile
3)Request for call back or order via our social networking pages like facebook, twitter, google+
4)Request for call back or order via whatsapp….whatsapp number is
5)Request for call back or order via e-mail ,please contact us at gopal@genomics.cn or healthchecker33@yahoo.com
6)Request for call back or order via SMS . type “NIFTY” send it to mobile number +919740513782/
Steps involved in order 2 report stages
1) place order via above any methods
2) we come n collect blood sample at your doorstep/clinic/hospital
3) send sample for processing at lab
4) after releasing report, we send report to your home/mail/smartphone/doctor as per your request.
We cover n collect orders from all over india.
Note- NIFTY is official trademark and license  of BGI
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