Service DescriptionNIPTiva Brilliant at Primea Polyclinic is an advanced non-invasive prenatal test analyzing cell-free fetal DNA from maternal blood. This comprehensive panel screens for autosomal trisomies, sex chromosome aneuploidies, fetal sex, microdeletions, and includes targeted screening for common single-gene monogenic conditions (e.g., cystic fibrosis, spinal muscular atrophy, Wilson's disease, Duchenne muscular dystrophy). Recommended for comprehensive genetic screening, families with monogenic disease histories, or high-risk screening results. Performed safely starting at 10 weeks of gestation without fasting.
