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  • MyDiagnostics Non Invasive Prenatal Screening Test - NIPT/NIPS - At Home
MyDiagnostics (NABL, CAP, ISO Lab)

Non-Invasive Prenatal Screening NIPS/NIPT Test - At Home

Rs. 21,000

Rs. 12,500

(0% Discount)

Test Parameters

NIPT Screening (Singleton)
  • Trisomy 21 (Down Syndrome) 
  • Trisomy 18 (Edwards Syndrome) 
  • Trisomy 13 (Patau Syndrome)
  • Turner Syndrome (Monosomy X/XO)
  • Klinefelter Syndrome (XXY)
  • Triple X (XXX)
  • Jacob's Syndrome (XYY)

Sample Required: Blood collected in Streak Tube - 10 ml.
Test Mode: At Home
Turn Around Time: 15 Days
Fasting Time: None
Other Instructions: We require Prescription, Ultra Sound report (USG), Dual and Quadruple Marker Report, Photo Identification Proof
Recommended for: At gestational age : 11 to 17 weeks.

 

About the Non Invasive Prenatal Screening Test - NIPT/NIPS

Non-invasive prenatal testing (NIPT) is a screening test that is used to assess the risk of certain chromosomal abnormalities in a developing fetus. NIPT is typically performed during the first or second trimester of pregnancy / gestational age 11 to 17 weeks, and is used to screen for conditions such as Down syndrome (trisomy 21), trisomy 13, and trisomy 18.

NIPT is a blood test that analyzes fetal DNA that is present in the mother's bloodstream. The test is considered to be non-invasive because it does not involve any risk to the fetus and does not require a procedure such as amniocentesis (a procedure in which a sample of amniotic fluid is taken for testing).

NIPT can provide valuable information about the risk of certain chromosomal abnormalities in a developing fetus. If the NIPT results indicate an increased risk of a chromosomal abnormality, the healthcare provider may recommend further testing to confirm the diagnosis.

NIPT test is offered in three variants - 

  • NIPT Basic
  • NIPT Advance 
  • NIPT Basic Twin

 NIPT does not test for the gender of the fetus

Whats the difference between NIPT Basic v/s NIPT Advanced

Basic screens for 5 Chromosomes

Advanced screens for 22 Chromosomes 

 

Pls ask for Sample report to confirm your requirements. 

Accuracy and Results of NIPT Test 

The accuracy of NIPT depends on several factors, including the stage of pregnancy, the specific condition being tested for, and the specific NIPT test being used.

Overall, NIPT has a high sensitivity (the ability to correctly identify individuals with the condition being tested for) and a high negative predictive value (the ability to correctly identify individuals without the condition). This means that NIPT is very good at identifying women who are at low risk of having a baby with a chromosomal abnormality.

There are several different NIPT tests available, and the specific test used will determine the results of the test. In general, NIPT results are reported as low risk or high risk for a specific chromosomal abnormality.

If the NIPT results indicate a low risk for a chromosomal abnormality, it means that the risk of the baby having the condition is very low. If the NIPT results indicate a high risk for a chromosomal abnormality, it means that the risk of the baby having the condition is higher than average

While not all tests are 100% accurate, the NIPT test will be able to provide critical insights on your pre-screening risk. You can get further testing done to determine whether your foetus is testing positive for a specific condition.


How is NIPT test performed   

The NIPT test is performed at a National Accreditation Board for Testing and Calibration Laboratories (NABL) certified laboratory. The sample collection is done at your residence, making it a highly convenient way of screening.

The blood sample is collected in a streak tube, about 10 ml, and your sample is then sent for quality testing and analysis. The technician will require basic details, such as Ultra Sound report (USG), Dual and Quadruple Marker Report, Photo Identification Proof, etc.    

Is NIPT recommended for all pregnant women?

NIPT is not recommended for all pregnant women, but it may be offered to women who are at increased risk of having a baby with a chromosomal abnormality due to their age or other risk factors. It is important to discuss the benefits and limitations of NIPT with a healthcare provider to determine if the test is right for you

 

  • The woman is above 30 years of age.
  • A high risk for abnormality is found through serum screening.
  • Certain abnormalities on ultrasound are identified.
  • There is a family history of chromosomal conditions or birth defects.
  • Couples have had a child with a chromosomal disorder.
  • A couple has a history of infertility or pregnancy loss (miscarriages or stillbirths)

 

 

About the Quality

Quality assurance is done at 3 levels 

  • Sample collection from home using one time sealed QR coded sterile kits and transportation to the lab including the temperature condition requirements 
  • Sample acceptance and QC at the lab 
  • Sample run at the NABL/CAP/ISO certified labs - Medgenome 

Who is it for ?

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What should I do after the test?

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What will I discover through this test?

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Guidelines

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FAQs

What is NIPT test?

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NIPT or non-invasive prenatal screening is a comprehensive
prenatal testing solution that is designed for screening of chromosomal
abnormalities. The NIPT blood test checks for abnormalities in a developing
foetus, and analyses fragments of foetal DNA in the mother's blood. You can
check the risk factor for Down syndrome, trisomy 18, and trisomy 13, among
other conditions, in a complete NIPT test in pregnancy health screening.

How accurate is the NIPT test for Down syndrome?

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Is the NIPT test done in India?

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How do I prepare for the NIPT test?

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When is the NIPT test done?

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What if NIPT test is positive?

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Which week is best for NIPT test?

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Is NIPT test necessary in pregnancy?

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What is the cost of NIPT test in India?

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Can we know the gender in an NIPT test?

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Does NIPT detect autism?

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Can NIPT detect birth defects?

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How do you read a NIPT test report?

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How do I buy an NIPT test in India?

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