{"id":101,"date":"2019-07-31T11:23:45","date_gmt":"2019-07-31T05:53:45","guid":{"rendered":"https:\/\/www.genes2me.com\/blog\/?p=101"},"modified":"2026-03-31T11:19:25","modified_gmt":"2026-03-31T11:19:25","slug":"non-invasive-prenatal-test-nipt-risk-free-pregnancy-testing-now-in-india","status":"publish","type":"post","link":"https:\/\/genes2me.com\/blog\/2019\/07\/31\/non-invasive-prenatal-test-nipt-risk-free-pregnancy-testing-now-in-india\/","title":{"rendered":"Non Invasive Prenatal Test : NIPT \u2013 Risk Free Pregnancy Testing now in India."},"content":{"rendered":"\n
\"NIPT
Know the baby’s risk towards any genetic abnormalities with NIPT Pregnancy Testing in India. <\/figcaption><\/figure>\n\n\n\n

Chromosomal\nAbnormalities Covered in ClariT NIPT<\/strong><\/p>\n\n\n\n

A barrage of information comes your way when a woman discovers that she\u2019s expecting. This includes making early and precise decisions about the health of the baby. With the advancement in technology and targeted test solutions, Did you know that you can detect genetic abnormalities that may arise during the pregnancy itself ? Let\u2019s understand how. NIPT testing in India is available in top locations of the country. <\/p>\n\n\n\n

Being one of the most trusted and emerging space in prenatal screening – Non Invasive Prenatal Testing<\/a><\/strong>, allows us to obtain baby\u2019s genetic information without affecting the baby. It is a Risk Free Genetic Test with an accuracy of ~99.9% to check for chromosomal abnormalities including Trisomy 21, 18, 13 and other chromosomal aneuploidies.<\/p>\n\n\n\n

ClariT NIPT, we easily detects the baby\u2019s\nhealth before his or her birth.<\/p>\n\n\n\n

What is\nChromosomal Abnormality?  <\/strong><\/p>\n\n\n\n

Normally, there are total 46 chromosomes in\nevery baby. 23 of the chromosomes are received from the mother and 23 from the\nfather. However, in\ncertain cases, a baby might be born with an extra or a missing chromosome,\nwhich can result in developing a chromosomal condition in the baby.<\/p>\n\n\n\n

ClariT NIPT looks for chromosomal abnormalities\nwhich primarily includes trisomy 21, trisomy 18, trisomy 13 and extra or\nmissing copies of the X and Y chromosomes.<\/p>\n\n\n\n

Trisomy 21 (Down\u2019s Syndrome)<\/strong><\/p>\n\n\n\n

Down syndrome has a high occurrence rate of 1\nin 800 births, which means around 32,500 babies with Down syndrome are born in\nIndia every year which is the highest number in the world. <\/p>\n\n\n\n

Babies\nborn with Down syndrome have an extra copy of chromosome 21, which manifests as\ndevelopmental delays, learning disabilities and low muscle tone. In addition,\nthey are also at risk for associated health issues like Alzheimer disease,\nheart problems, hearing loss or thyroid problems.<\/p>\n\n\n\n

Trisomy 18 (Edwards Syndrome)<\/strong><\/p>\n\n\n\n

This\nchromosomal condition occurs in about 1 in every 6,000 births. Edwards syndrome\noccurs when a baby has a partial or complete duplication of chromosome 18.\nNormally babies that are diagnosed with Edwards’s syndrome do not survive full\nterm because of the wide range of complex medical conditions associated with\nthe disorder. Babies that do survive birth have only a\nlittle chance of surviving their first year of life.<\/p>\n\n\n\n

Babies\nwith Edwards syndrome usually have a low birth weight, slow growth rate, a small-shaped\nhead and jaw, unusual shaped chest and severe delays in\ntheir mental development. They may also have kidney defects, heart issues,\nprotruding intestines etc. <\/p>\n\n\n\n

Trisomy 13 (Patau Syndrome)<\/strong><\/p>\n\n\n\n

This\nrare but severe condition occurs when a baby has three copies instead of two at\nchromosome 13. Patau syndrome occurs in about 1 in every 16,000 births and is\ndescribed by extreme development delays and advanced organ defects.<\/p>\n\n\n\n

Most\nbabies born with Patau syndrome generally struggle to endure in the first few\ndays of living, owing to a number of complications from related medical issues.\nBabies that do survive full term often have heart defects, brain and spinal\ncord abnormalities, structural eye defects and kidney problems. <\/p>\n\n\n\n

ClariT NIPT screens for abnormalities from chromosome 1 to chromosome<\/a> 22 <\/a>and also for sex chromosome X and Y. <\/p>\n\n\n\n

In\nSex Chromosome Aneuploidies it covers <\/p>\n\n\n\n

 XO<\/strong>(\nTurner Syndrome)<\/p>\n\n\n\n

 <\/strong>XXY <\/strong>(Klinefelter\nSyndrome)<\/p>\n\n\n\n

 XXX <\/strong>(Triple\nX Syndrome)<\/p>\n\n\n\n

 <\/strong>XYY <\/strong>(Jacobs\nSyndrome)<\/p>\n\n\n\n

Unfortunately, these conditions cannot be prevented. However, it can be detected before the baby is born. Conducted after the 9th\u00a0 <\/sup>week of pregnancy upto the 20th<\/sup> week \u2013 giving families plenty of time to prepare. ClariT NIPT provides assurance to expectant parents with accurate genetic <\/a>information during the pregnancy. <\/p>\n\n\n\n


Healthy Babies with ClariT NIPS Pregnancy Test, Now in India!<\/strong> <\/h2>\n\n\n\n

Know More: G2M<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"

Chromosomal Abnormalities Covered in ClariT NIPT A barrage of information comes your way when a woman discovers that she\u2019s expecting. This includes making early and…<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":[],"categories":[1],"tags":[107,67,66,106,71,105,108],"yoast_head":"\nNIPT Testing Solutions During Pregnancy - NIPT and NIPS Kits<\/title>\n<meta name=\"description\" content=\"NIPT testing - NIPS looks for chromosomal trisomies and other potential genetic disorders in the developing baby. 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