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*
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*The laboratory recommends the above gestational ages; the actual appropriate testing time should be confirmed after evaluation by the doctor.
Advantages
✔️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:
- Doctor Consultation
- Ultrasonography Examination
- 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)