• WHEN YOU’RE EXPECTING,
    YOU NEED CLARITY, NOT ADVICE.

    Know your baby’s genetic health through
    a safe, non-invasive test

Expecting Parents

When you’re expecting, you want to be assured of your baby’s health at every step of the journey. And this assurance comes when you get clear answers to your uncertainties.

MedGenome Claria, gives you the best reassurance with the aid of a unique combination of expert prenatal genetic counselling along with the world’s leading non-invasive prenatal screening test: MedGenome Claria. So you not only have an expert advisor guiding you through the entire process of understanding your baby’s genetics, but you also get all the vital information about your baby’s health from as early as the 9th week of your pregnancy.

As an expecting parent, you have a lot of worries, and the genetic health of your baby should not be one of them. MedGenome Claria helps ease your anxieties and allows you to make informed decisions about your baby under expert guidance.

What is MedGenome CLARIA?

MedGenome CLARIA is India’s first prenatal screening solution that combines expert genetic counselling with the highly accurate SNP based Panorama NIPT, that not only delivers near 100% accurate information about a baby’s genetic health (as early as the 9th week), but also at an incredibly absolute 0% risk to the baby and the mother.

Panorama NIPT

Panorama NIPT is a simple and safe, non-invasive prenatal screening test of the maternal blood that screens for your baby’s risk for genetic disorders from as early as the 9th week of your pregnancy.It screens for the most common genetic conditions such as Down syndrome, Edwards Syndrome, Patau Syndrome, Microdeletions etc. Additionally Panorama NIPT is the only NIPT to test for Triploidy.

When you are pregnant, some of the foetal DNA circulates in your blood stream. MedGenome Claria uses special DNA technology to separate the maternal DNA from the foetal DNA, which lets us screen for chromosomal abnormalities more accurately than other methods.

THE PROCESS

First, a small sample of blood is drawn from the mother’s arm. Being a non-invasive procedure, it poses no risk to the baby or mother. The sample is then sent to our Lab, ensuring faster results as compared to other providers in the country, to help ease your anxieties. You will receive your personalized results within 7-10 days.

Our expert genetic counsellors will be available for you and assist you with understanding the test and its implications better. MedGenome Claria offers both pre-test and post-test genetic counselling as an absolutely free service, so you have our assured support throughout the process.

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of the test

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ASK YOUR DOCTOR ABOUT MEDGENOME CLARIA

Call our toll-free number 1800-103-7590, or simply SMS ‘CLARIA’ to 56767 to get a free counselling session with one of our expert geneticists to help you understand the importance of prenatal screening and locate the sample collection center nearest to you.

MedGenome is PC & PNDT certified company by the Government of India.
MedGenome Claria does not disclose or test for gender determination.

Lifecycle
of the test

Step

QUICK AND SIMPLE BLOOD DRAW

A small sample of blood is collected from the mother’s arm.

Panorama NIPT is a non-invasive prenatal screening test and therefore poses no risk to the baby or mother.

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of the test

Step

RECEIVE YOUR PERSONALISED REPORT

MedGenome is the only company that performs the entire testing and reporting process within India. You will receive your personalised report within 7 to 10 days.

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of the test

Step

REVIEW YOUR TEST RESULTS

Your gynaecologist will give you a detailed analysis of the report, to help you understand your results better.

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of the test

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WE ARE HERE FOR YOU

If you need any further guidance with your report, you can call us and we will ensure that one of our genetic counsellors gets in touch with you.

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WHO NEEDS MEDGENOME CLARIA?

Every anxious mother faces a certain degree of risk. Internationally medical societies support the use of NIPT as the first-line screening for all pregnancies, irrespective of age factor or risks. However there are some factors that can put you and your baby at a higher risk for genetic disorders. These include:

  • An abnormal ultrasound
  • You and your partner are related - such as first cousins or close blood relatives.
  • Previous baby or pregnancy with a genetic disorder
  • Have a child who is affected with a genetic condition and are thinking about having another child in the future.
  • Have family members with mental retardation or birth defects
  • Have a history of infertility or pregnancy losses (miscarriages or stillbirths)
  • Are concerned that your health or lifestyle poses a risk to the pregnancy
  • Are concerned about risks to the pregnancy associated with increasing parental age
  • Received abnormal prenatal screening or ultrasound results
  • Are pregnant and the baby has been diagnosed with a birth defect or genetic condition
  • Family history of chromosomal conditions
  • Bad obstetric history
  • Existing chronic conditions like diabetes, etc
  • Maternal age of mid thirties and above.
  • You’re concerned that your health or lifestyle poses a risk to the pregnancy
  • You've used alcohol or drugs prior to or during your pregnancy.
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CHROMOSOMAL ABNORMALITIES

A chromosomal abnormality is when there’s a missing chromosome (monosomy), extra chromosome (trisomy) or a missing piece of a chromosome (microdeletions). A Chromosomal anomaly usually occurs when there’s an error during cell division.

This could lead your baby to develop certain chromosomal disorders such as Down Syndrome or Patau Syndrome, and affect their normal development.

Know More

RELIABILITY & ACCURACY

Our expert genetic counsellors will be available to guide you every step of the way, from helping you understand the test to reviewing and explaining the test results to give you the clarity you need.

Panorama NIPT can safely detect the possibility of genetic abnormalities in your baby with over 99.9% accuracy. It detects conditions that other tests can’t, including molar pregnancy, triploidy and vanishing twin.The test screens for Down syndrome with an accuracy rate that is greater than 99%.

It is the only test that differentiates between maternal and fetal DNA, which helps avoid false positives.The test has the highest sensitivity for 22q11.2 deletion syndrome, a common and potential severe micro-deletion that impacts women equally regardless of age.

CONDITION First Trim. Screen [6] Sensitivity | False Positive Rate PANORAMA NIPT [3,7] Sensitivity | False Positive Rate
Trisomy 21
Down’s Syndrome

79%
5%

99.9% [83/83]
0%

Trisomy 18
Edwards Syndrome

80%
0.3%

96.4% [27/28]
0.1%

Trisomy 13
Patau Syndrome

50%
0.3%

99% [13/13]
0%

Monosomy X
Turner Syndrome

Does not screen for

92.9% [13/14]
0.1%

Triploidy

Does not screen for

99% [8/8]

Optional Microdeletion Syndromes

22q 11.2 deletion
DiGeorge Syndrome *

Does not screen for

95.7% [45/47]

Additional Microdeletion *

Does not screen for

93.8% - 99%

* Additional Microdeletion includes: Angelman, Cri-du-Chat, 1p36 deletion & Prader-Willi

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WHY MEDGENOME CLARIA?

The MedGenome Claria Advantage:
  • Free genetic counselling with specialists
  • No risk of miscarriage or harm to the baby
  • Safer than traditional screening methods
  • The results are over 99.84% accurate
  • Uses the SNP-based method to find abnormalities in the baby
  • Rigorous validation and peer reviews
  • Screens a wider spectrum of genetic disorders, including Triploidy
  • Only fully validated NIPT in India
  • Quicker results with state-of-the-art central lab in India
  • Only prenatal screening test that screens for Triploidy
False Positive Rate Detection Rate
PANORAMA NIPT 0.005% 99.8%
Traditional Test 5% 65%

False Positive Rate (FPR) for MedGenome NIPT is less than 1% as compared to 5% False Positive Rate (FPR) of Maternal Serum Screening Test.

Book Your Test today and get to know about your baby’s health!

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DOCTOR TESTIMONIALS

"Excellent. This solves a riddle. I am utterly impressed. Thanks a lot!"

- Dr. Kausik, Genetics Department, Sanjay Gandhi Post Graduate Institute of Medical Sciences

"In my opinion, MedGenome represents a true spirit of scientific services at a reasonable price meeting the goal of social services through genomics"

- Dr. Jayesh Sheth,, Chairman, Institute of Human Genetics, FRIGE House

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PARENT TESTiMONIALS

"During my first pregnancy, my gynae recommended that I get some tests done as my age put the fetus at a high risk for Down’s syndrome. At the time, there was only invasive screening available. The experience wasn’t good, and caused me a bit of trouble. Last year, during my 2nd pregnancy, MedGenome NIPT was around. The test is non-invasive, so I wasn’t afraid to get it done. The test gave me and my family the much-needed peace of mind. My second baby is a healthy baby girl."

- Shreya Indulkar , 38

"I’d recommend all moms-to-be to go for the MedGenome NIPT. I think it’s a privilege to get any information about the risks your baby could be facing. I was particularly pleased with the support we got from MedGenome’s Genetic Counseling Team."

- Asha N. , 28

"My age posed a high risk for pregnancy, so my doctor suggested me to go for NIPT prenatal screening test. I was a bit doubtful, as I had never heard about this test before. However, thankfully on her insistence, I took the test, which helped me take corrective measures quite early. My baby is hale and hearty. I would highly recommend this test to all mothers-to-be out there. It is worth it!"

- Radha Mane , 36

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Book Your Test