NIPT(13,18,21, X, Y) in Mahuva

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NIPT(13,18,21, X, Y)
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FAQ

When should the NIPT test be done?

It can be done from 10 weeks of pregnancy up to delivery time. 

Which are the common sex chromosome conditions?

Turner syndrome, Klinefelter Syndrome, Triple X Syndrome and XYY Syndrome are the most commonly diagnosed sex chromosome conditions

How accurate are NIPT tests?

Factors such as multiple pregnancies, surrogacy, and obesity can affect NIPT results. This test is 99% accurate in detecting Down syndrome, though less accurate in detecting trisomy 18 and 13.

Why should I book a NIPT (13, 18, 21, X, Y) Test with Sterling Accuris ?

Sterling Accuris Diagnostics is at the forefront of pathology services in India and offers international quality standards. Our NABL-accredited laboratory specialises in providing quick and reliable diagnosis support for hospitals, physicians, and other healthcare facilities across the country. It is extremely convenient to book a NIPT (13, 18, 21, X, Y) Test in Mahuva with us that would give you accurate and precise results at a great price.

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.

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.

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.

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.

NIPT (13, 18, 21, X, Y) Test in Mahuva

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Sterling Accuris Diagnostics offers the NIPT (13, 18, 21, X, Y) Test in Mahuva to detect chromosomal abnormalities.

Overview of NIPT (13, 18, 21, X, Y) Test

This test detects foetal aneuploidy at chromosomes 13, 18, 21, X, and Y by analysing cell-free DNA in the maternal blood. It allows doctors to detect risks of genetic disorders like Down’s syndrome.

For an accurate diagnosis, you can head to Sterling Accuris Diagnostics for a NIPT (13, 18, 21, X, Y) Test in Mahuva.

Why and When is a NIPT (13, 18, 21, X, Y) Test Done?

The non-invasive prenatal test (NIPT) is done to detect chromosomal disorders caused by the presence of an extra or missing copy (aneuploidy) of a chromosome. It detects Down syndrome, which is caused by an extra chromosome 21, trisomy 18 which is caused by an extra chromosome 18, trisomy 13 which is caused by an extra chromosome 13, and extra or missing copies of the X and Y chromosomes, which are the sex chromosomes. 

This test is conducted when there are:

  • Abnormal ultrasound findings
  • A chromosomal disorder present in either genetic parent of the baby
  • Previous pregnancy with a chromosomal abnormality
  • Positive findings in biochemical markers

Sterling Accuris Diagnostics runs a NIPT (13, 18, 21, X, Y) Test in Mahuva that is highly sensitive and provides accurate results. If you are regarded as an “at-risk” patient, this testing is crucial.

NIPT (13, 18, 21, X, Y) Test: Main Highlights

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

How to Interpret the NIPT (13, 18, 21, X, Y) Test Report

The NIPT test can determine the presence or absence of any of the following:

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

Microdeletions

  • 3 deletion (Wolf-Hirschhorn syndrome)
  • 5p deletion (Cri-du-chat syndrome)
  • 2 (Prader-Willi syndrome/ Angelman syndrome)
  • 2 deletion (DiGeorge syndrome)

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