Non-Invasive Prenatal Testing (NIPT)

Non Invasive Prenatal Test – NIPT uses advanced whole genome sequencing to screen for common chromosomal abnormalities with high accuracy. This non-invasive test provides early detection and includes information about the fetal gender. Results are available in 7 days.

Recommended gestational age

10 – 21 Weeks

DETECTION RATE

Fetal Gender

99.76%

Trisomy 21

99.78%

Trisomy 18

99.84%

Trisomy 13

99.88%

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NIPT

Non-Invasive Prenatal Testing (NIPT)

NIPT 5 Chromosome

฿10,500
฿ 9,000

Comprehensive in 5 Chromosome

  • Fetal Gender
  • Singleton / Twin
  • Natural / IVF
  • Down syndrome(Trisomy 21)
  • Edwards’ syndrome (Trisomy 18)
  • Patau’s Syndrome (Trisomy 13)
  • Sex Chromosome abnormally
    ( XO, XYY, XXY, XXX )
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NIPT All Chromosome

฿14,500
฿ 12,500

Comprehensive insights in All Chromosome

  • Fetal Gender
  • Singleton / Twin
  • Natural / IVF
  • Down Syndrome (Trisomy 21 )
  • Edvards’ Syndrome (Trisomy 18)
  • Patau’s Synsrome (Trisomy 13)
  • Sex Chromosome abnormally
    ( XO, XYY, XXY, XXX )
  • Trisomy 8, 9, 16, 22
  • Other chromosome
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NIPT at Home

With Medpro, enjoy the convenience of home or hotel health tests for just ฿800. Experience quality care in the comfort of your own space—book your appointment now!

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Outside Bangkok

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For at-home tests, please provide your complete address

A Guide to Non-Invasive Prenatal Testing (NIPT)
What is Non-Invasive Prenatal Testing (NIPT)

NIPT, or Non-Invasive Prenatal Testing, is a screening method that analyzes small fragments of fetal DNA in a pregnant woman’s blood to assess the risk of genetic conditions, particularly chromosomal abnormalities like Down syndrome (trisomy 21), trisomy 18, and trisomy 13. It is non-invasive, posing no risk to the fetus, and is known for its high accuracy. Results are typically available within a week or two. NIPT is often recommended for women with higher risks, such as advanced maternal age or family history of genetic disorders. The sample type used is a blood sample from the mother.

Conclusion

NIPT, or Non-Invasive Prenatal Testing, is a screening method that analyzes small fragments of fetal DNA in a pregnant woman’s blood to assess the risk of genetic conditions, particularly chromosomal abnormalities like Down syndrome (trisomy 21), trisomy 18, and trisomy 13. It is non-invasive, posing no risk to the fetus, and is known for its high accuracy. Results are typically available within a week or two. NIPT is often recommended for women with higher risks, such as advanced maternal age or family history of genetic disorders. The sample type used is a blood sample from the mother.

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Such as Copper, Iron, Methanol, Zinc, Aluminum, and more. Packages are available for both blood and urine samples to detect potential metal imbalances or toxicities.

NIPT

Discover chromosomal abnormalities like Down’s syndrome Edwards’ syndrome Patau’s Syndrome Fetal Gender and other Chromosome

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