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Prenatal tests are important before the birth of the baby. Here's what couples should know

Published on: Apr 14, 2023, 19:34:45 IST
By , Delhi
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Prenatal tests are important before the birth of the baby. Here's what couples should know (Photo by Kelly Sikkema on Unsplash)
Prenatal tests are important before the birth of the baby. Here's what couples should know (Photo by Kelly Sikkema on Unsplash)
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The couple is often advised to opt for non-invasive prenatal tests. Here's all that parents need to know

The couple is often advised to opt for non-invasive prenatal tests (NIPT) and parents often have queries related to the benefits of prenatal screening and to making an informed choice to better understand the health status of the baby but you should not worry anymore as we tell you everything you want to know about this test. NIPT, also known as non-invasive prenatal screening (NIPS), helps to know the risk that the foetus will be born with certain chromosomal disorders, such as Down syndrome (trisomy 21).

In an interview with HT Lifestyle, Dr Priya Deshpande, Consultant Foetal Medicine at Motherhood Hospital in Kharghar, explained, “By doing this test, it is possible to know if there is high risk of the baby having any chromosomal abnormalities. This test will detect small fragments of DNA that are circulating in a pregnant woman’s blood, which is called cell-free DNA (cfDNA).”

She elaborated, “NIPT is non-invasive as it is done by taking blood from the pregnant woman to test whether a foetus has a genetic condition and does not pose any risk to the foetus. This test is a boon as it will help the couple to relax and understand the baby’s health.”

Revealing who should opt for NIPT, she said, “Non-Invasive Prenatal Testing (NIPT) is important for pregnant women during pregnancies. It can be done by singleton pregnancies, twin pregnancies, and in vitro fertilization (IVF) pregnancies.” Talking about the conditions that are screened for NIPT, she said, “Conditions such as Trisomy 21, Trisomy 18, Trisomy 13, Sex Chromosome Aneuploidies (XO, XXY, XXX, XYY), Rare Autosome Aneuploidies (Trisomy 9, Trisomy 16, Trisomy 22) can be screened with the help of this test. This test screens the high-risk foetuses with 99% sensitivity for Trisomy 21. In case of high risk further invasive tests like chorion villous biopsy or amniocentesis are recommended to have a definitive diagnosis.”

 
ABOUT THE AUTHOR
Zarafshan Shiraz

A lifestyle aficionado with a knack for crafting engaging news across fashion, health, relationships, art and culture, travel, recipes, festivals and pets. Always ahead of the curve, with a finger on the pulse of the latest trends and a passion for storytelling, I bring vibrant, informative and captivating content to life that ensures you stay inspired and in-the-know.

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Catch every big hit, every wicket with Crick-it, a one stop destination for Live Scores, Match Stats, Quizzes, Polls & much more. Explore now!.

Catch your daily dose of Fashion, Taylor Swift, Health, Festivals, Travel, Relationship, Recipe and all the other Latest Lifestyle News on Hindustan Times Website and APPs.
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