non-invasive-prenatal-screening

Non Invasive Prenatal Screening

Early Intervention, Healthy Babies!

NIPS is a non invasive test, performed on cfDNA that screens Ultrasound abnormalities and chromosomal abnormalities identified by other screening tests.

 

non-invasive-prenatal-screening
When is NIPS advisable ?
When is NIPS advisable ?

NIPS is advisable when -There are concerns about chromosome abnormalities in your pregnancy.

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NIPS is advisable when 

  • Ultrasound abnormalities have been identified .
  • You have had earlier abnormal screening results for this pregnancy.
  • You, your partner, or a prior pregnancy or child were identified with a chromosome abnormality.
  • You have received inconclusive results from another fetal DNA screening test.
ClariT
ClariT

Screens for most common trisomies including Trisomy 21,18,13 and sex chromosome aneuploidies. It provides aneuploidy information of all the other remaining chromosomes.

Price: ₹21000.00
MaterniT Genome
MaterniT Genome

Because every chromosome matters, we analyze them all to get Karyotype level details.

Price: ₹70000.00

Comparison

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 Trisomy/Monosomy  Trisomy 22
     Select Microdeletions
     Sex Chromosome Aneuploidy

 

MyFitBabyPlus

Stepping into Motherhood ?
MyBabyFitPlus
Benefits

FREE Sample Collection

PAN India Logistics

Accurate Reporting

Fast TAT

Stringent QC

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MyFit Baby Plus
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