NIPT (24 Chromosomes) in Mansa

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NIPT (24 Chromosomes)
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FAQ

Can the NIPT test diagnose a genetic disorder?

No, NIPT is a screening test that can only provide insights into an unborn fetus’ risk of developing certain genetic conditions, and not diagnose the disease.

When should the NIPT test be done?

Hence optimum results are obtained after 10 weeks of gestation. Generally, there is not enough fetal DNA in a pregnant woman’s blood before 10 weeks of gestation.

Why should I seek a NIPT (24 Chromosomes) Test with Sterling Accuris

Sterling Accuris Diagnostics specialises in providing quick and reliable diagnosis support for hospitals, physicians, and other healthcare facilities across the country.

It is convenient to book a NIPT (24 Chromosomes) Test in Mansa with us which would give you accurate and precise results at a great price. We also offer a safe home collection for your convenience.

Why the test is considered non-invasive?

NIPT is a safe and non-invasive alternative to testing for fetal abnormalities during pregnancy, requiring only the mother's blood sample without risk of harm or discomfort to her unborn child. The test measures the fetal DNA which is circulating in the mother’s blood during the period of pregnancy. 

What makes Sterling Accuris a better pathology lab than others?

For us, precision care, safe sample collection, timely delivery of reports, and precise reporting of patient results while adhering to health and safety precautions are the cornerstone of our success.

What other packages does Sterling Accuris offer?

Sterling Accuris offers a range of packages including Senior citizen (male and female) package, healthy heart profile, diabetes profile, vitamin profile, covid immunity package and much more. Visit our website to learn more about these packages.

How long does it take to receive test results?

Though most tests are completed and reported within about 24 hours of receiving the sample for testing, certain tests take several days to weeks.

Your soft copy will be sent on registered email id and Whatsapp. Also, you will receive SMS with link to download your report. Also, your report is available on our website / app.

To know the status of the report, you can call our customer care team on 812 813 0000.

Is there any preparation or precautions for patient before tests or body checkup?

Fasting maybe required in case of a few tests to ensure accurate results. 

In general, it is also advisable to abstain from alcohol and heavy diet at least for 24 hours before any health test. You can see the requirement for each test on the product page on our website / app.

Do you provide home visit/collection service?

Yes. We do provide home collection services at your doorstep.

Please go ahead and book your visit today from our top menu options in this website / chat or do call us on 812 813 0000.

NIPT (24 Chromosomes) Test in Mansa

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Sterling Accuris Diagnostics offers the NIPT (24 Chromosomes) Test in Mansa  to provide important information about chromosomal abnormalities.

Overview of NIPT (24 Chromosomes) Test

Non-invasive Prenatal Testing (NIPT) offers expectant parents an advanced method of genetic screening, allowing them to detect chromosomal abnormalities such as trisomy 21, 18 and 13. In addition, this test screens all 24 chromosomes and is able to uncover rarer anomalies including autosomal disorders. 

For an accurate opinion, you can head to Sterling Accuris Diagnostics for a NIPT (24 Chromosomes) Test in Mansa.

Why and When is a NIPT (24 Chromosomes) Test Done?

NIPT is a test that can detect chromosomal disorders, where either extra or missing copies of chromosomes are present (aneuploidy).  It detects Down syndrome (trisomy 21), Edward Syndrome (trisomy 18) and trisomy 13 (Patau Syndrome), and extra or missing copies of the X and Y chromosomes, which are the sex chromosomes. It offers a comprehensive screening for extra chromosomal conditions, caused by the absence or duplication of sections in chromosomes. It is also being used to detect genetic disorders stemming from alterations in single genes.

This test is conducted when there are:

  • An abnormal ultrasound finding
  • A chromosomal disorder in either parent 
  • Previous pregnancy with a chromosomal abnormality
  • A positive finding in biochemical markers 

Sterling Accuris Diagnostics runs a NIPT (24 Chromosomes) Test in Mansa that's largely sensitive and provides accurate results. However, this testing is strongly recommended, especially if you're regarded as an “at-threat” case.

NIPT (24 Chromosomes) Test: Main Highlights

  • Instructions: Fasting is not required 
  • Recommended For: Pregnant females 
  • Sample Type for Test: Blood in W. B Streck Tube

How to Interpret the NIPT (24 Chromosomes) Test Report

The result shows either an increased or decreased risk for a foetus to have any of the following conditions:

Chromosome abnormality

Interpretation

Trisomy 21

Down syndrome: Characterised by intellectual disability, distinctive facial features, and musculoskeletal impairments during infancy.

Trisomy 18

Edwards Syndrome: Characterised by intrauterine growth retardation and abnormally shaped head.

Trisomy 13

Patau Syndrome: Characterised by intellectual disability, many physical defects

Sex chromosome aneuploidies

  • Monosomy X (Turner syndrome)
  • Trisomy X (Triple X syndrome)
  • XXY (Klinefelter sydrome)
  • XYY syndrome

Abnormalities in other chromosomes

Detects disorders caused by translocations, deletions, duplications, inversions, etc

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