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.

From 10 Weeks

DETECTION RATE

Gender

99.76 %

Trisomy 21

99.78 %

Trisomy 18

99.84 %

Trisomy 13

99.88 %

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Open Daily 09:30 – 19:00

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NIPT PACKAGE

NIFTY

NIFTY NIPT Basic

5 Chromosome


Promotional Price

฿9,000
฿ 8,250

Comprehensive 5 Chromosome

  • Fetal Gender
  • Singleton
  • Natural / IVF
  • Down Syndrome (Trisomy 21 )
  • Edvards’ Syndrome (Trisomy 18)
  • Patau’s Synsrome (Trisomy 13)
  • Sex Chromosome abnormally
    ( XO, XYY, XXY, XXX )

NIFTY NIPT Standard

23 Chromosome


Promotional Price

฿12,500
฿ 11,250

Comprehensive insights in All Chromosome

  • Fetal Gender
  • Singleton
  • 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

NIFTY NIPT Advance

23 Chromosome

with 92 Deletion & Duplication


Promotional Price

฿17,500
฿ 16,250

Comprehensive insights in All Chromosome

  • Fetal Gender
  • Singleton
  • 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
  • 92 Deletion and Duplication

NIFTY NIPT Twin

5 Chromosome

For Twin Pregnant


Promotional Price

฿15,500
฿ 14,250

Comprehensive 5 Chromosome

  • Detection Chomosome Y
  • Twin pregnant
  • Natural / IVF
  • Down Syndrome (Trisomy 21 )
  • Edvards’ Syndrome (Trisomy 18)
  • Patau’s Synsrome (Trisomy 13)

NIPS-NGD

NGD NIPT 5C

5 Chromosome


Promotional Price

฿9,000
฿ 8,250

Comprehensive 5 Chromosome

  • Fetal Gender
  • Singleton
  • Natural / IVF
  • Down Syndrome (Trisomy 21 )
  • Edvards’ Syndrome (Trisomy 18)
  • Patau’s Synsrome (Trisomy 13)
  • Sex Chromosome abnormally
    ( XO, XYY, XXY, XXX )

NGD NIPT Plus

23 Chromosome

with 47 Deletion & Duplication


Promotional Price

฿15,500
฿ 14,250

Comprehensive insights in All Chromosome

  • Fetal Gender
  • Singleton
  • 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
  • 47 Deletion and Duplication

Panorama NIPT

Panorama NIPT singleton

5 Chromosome


Promotional Price

฿17,500
฿ 16,250

Comprehensive 5 Chromosome

  • Fetal Gender
  • Singleton
  • Natural / IVF
  • Down Syndrome (Trisomy 21 )
  • Edvards’ Syndrome (Trisomy 18)
  • Patau’s Synsrome (Trisomy 13)
  • Sex Chromosome abnormally
    ( XO, XYY, XXY, XXX )

Panorama NIPT Twin

5 Chromosome


Promotional Price

฿19,250
฿ 18,250

Comprehensive 5 Chromosome

  • Detection Chromosome Y
  • Twin pregnant
  • Natural / IVF
  • Down Syndrome (Trisomy 21 )
  • Edvards’ Syndrome (Trisomy 18)
  • Patau’s Synsrome (Trisomy 13)

Because every mom deserves peace of mind — from the very beginning.

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!

Timely Care for Better Health

Book now

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 represents a major advancement in prenatal care, enabling early detection of conditions like Down syndrome, Edwards syndrome, and Patau syndrome. By analyzing fetal DNA in the mother’s bloodstream, this non-invasive screening offers valuable insights that inform parental decision-making and care strategies. Early identification of potential genetic disorders not only helps families prepare for their journey but also enhances the support available to them, ultimately contributing to healthier outcomes for both parents and children.

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