15% Off on NIPT Test Cost – Starting From ₹17100 Only

Lowest NIPT test cost in India!
Lowest NIPT test cost in India!

NIPT (Non-Invasive Prenatal Testing), also known as Harmony Test or Panorama test, is done to detect fetal chromosomal abnormalities indicating the likelihood of the baby born with genetic disorders like Down syndrome, Patau syndrome, Edwards syndrome, and Turner syndrome.

Book your NIPT test at your local top-quality labs through us at up to 15% discount. The lowest NIPT test cost is ₹17100 only.

NIPT Test in India Through LabsAdvisor

  • 1500+ NIPT tests conducted yearly
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  • 40+ lab options for NIPT test in India
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Book the NIPT test online yourself at any time of the day or night by clicking on the appropriate link in the table below.

NIPT Test Cost in India and Lab Details

We offer the NIPT test in over 20 Indian cities. Click on the link of your city below to choose a lab and make an online booking for home collection at a suitable time. 

City for NIPT TestPrices Starting From
NIPT Test Cost in Delhi₹17100
NIPT Test Price in Gurgaon₹17100
NIPT Test Price in Noida₹17100
NIPT Test Price in Mumbai₹27904
NIPT Test Cost in Bangalore₹27904
NIPT Test Cost in Chennai₹27904
NIPT Test Cost in Hyderabad₹27904
NIPT Test Price in Other Indian Cities₹17100

If your city is not listed in the table above, call us on 09811166231. We will get back to you with the NIPT test cost in India near your location.  

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The discounts on the NIPT test cost in India are available only to those who made the booking through LabsAdvisor.com. You will be asked to pay the actual NIPT test price if you do not carry the booking confirmation message sent by the LabsAdvisor.com
Uses of NIPT Test.
Uses of NIPT Test.

What is the science behind the harmony test?

During the pregnancy maternal blood carries cell-free fetal DNA which can be isolated and measured. The difference in the chromosomal build-up of that DNA is used to identify abnormalities.

Normally the DNA will have 23 pairs of chromosomes, 23 from the mother and the other 23 from the father. But sometimes instead of 46 chromosomes the DNA carries an extra copy of the chromosome or has a missing or structurally altered chromosome leading to some genetic conditions.

What is Down Syndrome or Trisomy 21?

Down Syndrome is a genetic disorder caused by the presence of all or part of the third copy (hence Trisomy) of chromosome 21. The physical features and medical problems associated with Down Syndrome vary in each child.

Some children may need a lot of medical help while others can lead healthier lives. It typically results in abnormal facial features, slant eyes, and small ears. The other characteristics are delayed development and intellectual impairment.

Risk of Down Syndrome.
Risk of Down Syndrome.

People with Down Syndrome also have an increased risk of pulmonary hypertension and congenital heart disease. Low muscle tone is also seen in cases of this syndrome, babies particularly may seem floppy. Other medical problems that may happen more frequently are

  • stomach and intestine problems
  • thyroid problem
  • seizures
  • breathing problems including asthma and sleep apnea
  • hearing or vision problems

Regular evaluations by ophthalmologists and audiologists are necessary for people with Down Syndrome. There is no cure for this syndrome but the health problems that go along with it can generally be treated.

Many resources and facilities are available to help children and their families living with this condition. Earlier the life expectancy of a person with Down Syndrome was around 18-19 years but due to increased awareness and medical advancement, it has increased considerably.

The likelihood of having a baby with Down syndrome increases with the mother’s age. A woman whose age is 20 has about 1 in 2000 chance of having a baby with Down syndrome, while a woman aged 40 has a 1 in 100 chance.

So older mothers should definitely undergo the NIPT screening for a well-informed and healthier pregnancy. Know more about Down Syndrome here.

What is Edwards Syndrome or Trisomy 18?

An extra copy of chromosome 18 causes a  serious disorder called Edwards syndrome. 94 % of babies with Edwards syndrome will have the full form which means that every cell in their body has three copies of chromosome 18.  Most of these babies die before infancy.

The less severe form is called mosaic trisomy but rarely babies survive into early adulthood. These babies are born with low birth weight along with a number of serious health issues.

The health problems include heart and kidney problems, feeding problems, breathing problems, and frequent infection of the lungs and urinary systems.  Around one in 12 babies live beyond one year but have severe mental disabilities.

Like Down Syndrome, there is no cure for Edwards Syndrome and symptoms can be very difficult to manage. Life-threatening issues such as infections and heart problems have to be regularly monitored.

For physical and mental abnormalities physiotherapy and occupational therapy are needed. A lot of support on both the medical and emotional front is required.

Edwards syndrome is rarely inherited. It is a random error in cell division so it is extremely unlikely that siblings will also be born with a similar abnormality.

The chances of having a baby with Edwards Syndrome increase with the mother’s age. So high-risk mothers should go for a prenatal screening test to make an informed choice to continue the pregnancy. To know more about this condition, you may check here.

What is Patau Syndrome or Trisomy 13?

The prevalence of extra chromosome number 13 instead of the usual pair causes this abnormality called Patau Syndrome. Many fetuses never survive until term or are stillborn. It also results in growth restriction and low birth weight. 80% of babies born with Patau Syndrome have a congenital heart defect.

As the brain does not divide into two halves, facial defects like cleft lip and palate can be present. Neural tube defects and severe learning disabilities are also signs of the disorder. Seizures and feeding difficulties are common.

If Patau Syndrome is due to structural chromosomal abnormality or unbalanced chromosomal translocation then both the parents need to undergo chromosomal analysis.

This is significant for future pregnancies as there is a higher chance of recurrence. Risk also rises with maternal age but not as significantly as in Down Syndrome and Edwards Syndrome.

Nevertheless, expectant mothers above age 35 or having a close family history of giving birth with Patau Syndrome should go for the NIPT screening. To know more about this abnormality, check here.

What is Turner Syndrome?

Turner Syndrome is a condition in which a female is completely or partly missing an X chromosome. While normal people have 46 chromosomes, people with Turner Syndrome will have 45.

The chromosomal abnormality may be present in some cells resulting in the less severe form with fewer symptoms. The common symptoms are short stature, webbed neck, low set ears, and reproductive sterility. Diabetes and heart defects occur more frequently resulting in shorter life expectancy.

Turner syndrome, unfortunately, has no cure.  Only symptomatic treatments are possible. A growth hormone injection is given to increase adult height. Thyroid hormone supplements are given to treat hypothyroidism.

As women with Turner Syndrome have an increased risk of type 1 diabetes in childhood and further developing type 2 diabetes in adult years, they are advised to maintain a healthy weight. One-third of women with Turner Syndrome have kidney problems but can be corrected surgically.

Women who are unable to conceive due to this condition may be able to use IVF or other fertility treatments.

In most cases, Turner syndrome is a random event so the risk to parents with a Turner Syndrome child having pregnancies with similar disorders is not increased.

In spite of less recurrence risk, screening and genetic counseling are often recommended for parents who have a pregnancy or a child with Turner Syndrome. To know more about this genetic abnormality, check here. 

What is NIPT (Non-invasive Prenatal Testing) procedure?

The NIPT test requires the drawing of blood from the expectant mother for testing at a lab. As no invasion of the fetus is involved there is NO risk of miscarriage.

The test is highly accurate (over 99.5%) and totally safe. However, NIPT is a screening test, which means if the result of the test is positive further diagnostic tests are carried out to confirm the disorder.

The test can be done anytime after the tenth week into pregnancy, typically between 10-24 weeks. The results are back in 6-7 days.

Who should get the NIPT Test / Panorama Test done?

The test is recommended for expectant mothers who are

  • Are first time pregnant and above 35 years of age
  • Has a family history of these conditions
  • Any other pre-natal test raises a concern

Since this test is not invasive and completely safe, doctors are recommending these tests more now. Check with your doctor if this test is required for you.

What is the significance of the Panorama test?

While traditional maternal blood tests miss detecting genetic abnormalities, NIPT accurately identifies more than 95% of cases. It also eradicates the risk of invasive testing for genetic disorders on low-risk mothers.

Only positive results need to undergo further testing. Also, it allows the parents the choice of continuing or terminating the affected pregnancy.

Other topics you may be interested in:-
  1. DNA Test Costs in India
  2. DNA Paternity Test Cost in India
  3. DNA Test for Relationship in India
  4. DNA Paternity Test During Pregnancy in India
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