Early Intervention, Healthy Babies!
ClariT NIPT (Non Invasive Prenatal Testing) is a non invasive genetic screening test, conducted through the mother's blood sample with no risk to the baby.
With an accuracy of >99% ClariT NIPT has become one of the most recommended screening tests by doctors and healthcare providers.
Get an insight into genetic abnormalities from as early as the ten week of pregnancy.
Know if the baby is subjected to any of the following genetic conditions during pregnancy
Trisomy 21 (Down’s syndrome) Trisomy 18 (Edwards’ syndrome) Trisomy 13 (Patau’s syndrome)
ClariT Lite screens for Trisomy 21, 18 & 13
Screens for most common trisomies including Trisomy 21,18,13 and sex chromosome aneuploidies. It provides aneuploidy information of all the other remaining chromosomes.
Because every chromosome matters, we analyze them all to get Karyotype level details. Screens for all chromosomal aneuploidies including Trisomy 21, 18, 13, SCA along with ~ 66 large deletions/duplications and 20 Micro-deletions/ Micro-duplications.
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• A women with advanced maternal age (>=35years)
• High Risk on Maternal Serum Screening
• Abnormal ultrasound findings
• History of a previous baby with Down’s syndrome
• Risk confirmation for Chromosomal abnormalities in Twin Pregnancy
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ClariT NIPT report provides you with the information which shows whether your baby is at a low-risk or high-risk of having a genetic disorder.
High Risk- A high risk result does not mean the baby has a chromosomal abnormality, rather, it indicates a very high probability that your baby may have that condition.
Low Risk- A low risk result indicates that it is very unlikely that your baby is affected by one of the conditions on the ClariT panel.
No Result- In a small percentage of cases, ClariT may not be able to obtain sufficient information from your blood sample to determine an accurate result. If this occurs, a second blood sample may be accepted.
| ClariT Lite (Validated in India) | ClariT (Validated in India) | MaterniT21 Plus (from Sequenom Labs, USA) |
| Trisomy 21 | Trisomy 21 | Trisomy 21 |
| Trisomy 18 | Trisomy 18 | Trisomy 18 |
| Trisomy 13 | Trisomy 13 | Trisomy 13 |
| Sex Chromosome Aneuploidy | Trisomy 16 | |
| Other Chromosome Aneuploidy | Trisomy 22 | |
| Select Microdeletions | ||
| Sex Chromosome Aneuploidy |
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