Genetic Test

Non-Invasive Prenatal Testing (NIPT) for Chromosomal Abnormalities

An extra copy of chromosome 21 causes Down syndrome within the human body's cells. Approximately one out of every 800 newborns is born with Down syndrome, and the chances increase with the age of the pregnant woman. It is the most common chromosomal abnormality and a genetic cause of intellectual disability. 

While Down syndrome cannot be effectively prevented, parents can assess the risk of their baby having Down syndrome through prenatal testing. This information can help families plan their pregnancies more comprehensively and prepare for the future care of their children.

Take care for your baby's health and take action now!

During pregnancy, a small amount of fetal cell-free DNA is present in the mother's blood. Non-Invasive Prenatal Testing (NIPT) is an advanced technique that analyzes the levels of this cell-free DNA to assess the risk of the fetus having Down syndrome or other chromosomal abnormalities, including Edwards syndrome, Patau syndrome, sex chromosome-related disorders, and microdeletion syndromes. NIPT is more accurate and comprehensive screening test compared to traditional screening methods for Down syndrome.

Testing Target*

  • Single fetal embryos: ≥ 10 weeks
  • Twin or reduced embryos: ≥ 12 weeks
  • Triple fetal embryos: ≥ 14 weeks
  • Suitable for artificially conceived embryos

*The laboratory recommends the above gestational ages; the actual appropriate testing time should be confirmed after evaluation by the doctor.


✔️Early Detection

The test can be performed as early as 10weeks of pregnancy, and results are typically available within 5-7 working days, providing a safe, quick and reliable option.

✔️ Simple Process, Safe

Only a 10ml blood sample from the pregnant woman is required, with no risk of miscarriage

✔️ High Accuracy rate

Over 99% for common chromosomal abnormalities

Genetic Test / Prenatal Care

Non-Invasive Prenatal Testing (NIPT) for Chromosomal Abnormalities

Led by Specialist in Obstetrics and Gynaecology
*(The price includes doctor's consultation fees, testing expenses, and ultrasound examinations.)

Service includes:

  1. Doctor Consultation
  2. Ultrasonography Examination
  3. MINA Safe T21 ExpressTM

Standard Version $6,800

  • Trisomies: 3 items
  • Sex Chromosome Aneuploidies: 4 items
  • Microdeletion Syndromes: 7 items

Advanced Version $7,800

  • Trisomies: 22 items
  • Sex Chromosome Aneuploidies: 4 items
  • Microdeletion Syndromes: More than 126 items (down to 3Mb Mircodeletion or Microdeplication Syndromes)

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