NIPT Test Screen for Fetal Chromosomal Abnormalities with a Safe, Non-Invasive Methodโ€”No Amniocentesis Needed

Know in advance to plan your pregnancy with confidence

Pregnancy is a significant journey filled with the hopes of the family. Knowing the health of your baby early in the pregnancy helps you prepare with confidence, safety, and informed decisions.

NIPT (Non-Invasive Prenatal Testing) is one of the advanced technologies that screens for fetal chromosomal abnormalities by taking a small blood sample from the mother, without the risks associated with amniocentesis, reducing anxiety while providing highly accurate results.

What is NIPT Test?

NIPT (Non-Invasive Prenatal Testing) is a non-invasive screening test that analyzes the cell-free fetal DNA (cfDNA) circulating in the motherโ€™s bloodstream.

This test can screen for chromosomal abnormalities such as:

  • Trisomy 21 (Down syndrome)
  • Trisomy 18 (Edwards syndrome)
  • Trisomy 13 (Patau syndrome)
  • Sex chromosome abnormalities
  • Fetal sex (if desired)

How is the Test Done?

  • A blood sample is drawn from the mother (approximately 10 mL).
  • The sample is then analyzed using advanced technologies like NGS (Next Generation Sequencing).
  • Results will be available within 7โ€“14 days.

Preparation for the Test

  • No fasting required before the test
  • Testing can be done from 10 weeks of pregnancy onwards
  • Please inform your doctor about any pregnancy history, previous miscarriages, or family history of fetal abnormalities
  • If pregnant with twins, inform your doctor to assess the suitability

Why Should You Get Tested?

  • Screen for common chromosomal abnormalities in the fetus
  • Know the fetal sex accurately early in the pregnancy (if desired)
  • Reduce the need for amniocentesis, which carries a risk to the fetus
  • Increase confidence in managing the pregnancy and planning for ongoing care
  • Provide safety and assurance for the family

Who Should Get Tested?

  • All pregnant women, especially those over the age of 35
  • Those with a family history of genetic disorders
  • Women who have experienced unexplained miscarriages
  • Couples with a history of having a child with chromosomal abnormalities
  • Pregnant women who do not wish to undergo the risks associated with amniocentesis

Summary

NIPT Test is a smart choice for modern mothers who want to plan their pregnancy safely, confidently, and with reduced risk. With just a small blood sample, you can get important information about your baby and plan further care appropriately.

At LINNA Clinic, we offer the NIPT Test with expert advice from our specialists, providing personalized care in conjunction with internationally accredited labs.

๐Ÿ“ To schedule your NIPT Test:
๐Ÿ“ฒ Line: @linnaclinic
๐Ÿ“ž Phone: 063-609-8888
๐Ÿ“ฑ WhatsApp: +66 91 979 9554

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18,000 THB

NIPT Test โ€” Non-Invasive Prenatal Screening for Chromosomal Abnormalities A safe and highly accurate DNA-based test that analyzes the babyโ€™s genetic information through a simple maternal blood draw. The NIPT screens for common chromosomal abnormalities such as Down syndrome, Edwards syndrome, and Patau syndrome โ€” providing early insight into your babyโ€™s health without any risk to mother or child.
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NIPT Test:

18,000 THB

Description: NIPT Test โ€” Non-Invasive Prenatal Screening for Chromosomal Abnormalities A safe and highly accurate DNA-based test that analyzes the babyโ€™s genetic information through a simple maternal blood draw. The NIPT screens for common chromosomal abnormalities such as Down syndrome, Edwards syndrome, and Patau syndrome โ€” providing early insight into your babyโ€™s health without any risk to mother or child.
Specimen: Blood in Streck Tube
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