NIPT Basic Prenatal Test | Lahalak Platform
Ensure your baby's health with total safety. This advanced screening analyzes fetal DNA from maternal blood to detect common chromosomal syndromes with high accuracy and zero risk.
Scientific name: Non-Invasive Prenatal Testing (NIPT Basic)
Non-invasive prenatal testing (NIPT BASIC) is an advanced molecular test based on next-generation sequencing (NGS) to detect fragments of fetal DNA (cffDNA) that are freely circulating in maternal blood plasma. The test aims to assess the risk of the fetus having the most common trisomy: trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), an...
Service type
Prenatal Genetic Screening
Duration
15-20 minutes
Fasting
Fasting is not required
Included Services
- Comprehensive examination and report for Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), Patau syndrome (trisomy 13), and sex chromosomal abnormalities (X, Y).
- Determining the sex of the fetus (upon request).
- Consult with a maternal-fetal medicine specialist or genetic counselor to interpret the overall results.
- Personal support services from Halak.
Medical Service Information
Conditions & Notices
- Fasting is not required. A normal blood sample is taken from the mother (plasma tube).
- The optimal time for the procedure is from the tenth week of pregnancy (10 weeks 0 days) onwards. The gestational age must be accurately confirmed by ultrasound.
- The doctor should be informed of the pregnancy history (single, twins), any previous fertility treatments (such as IVF), or recent blood transfusions.
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