UNITY Complete with Fetal Antigen NIPT
A combined maternal carrier and prenatal chromosome screen with added fetal-antigen information. The catalogue describes carrier screening with conditional single-gene NIPT follow-up alongside chromosome and fetal-antigen assessments. These are screening results, not a diagnosis.

AED 5,500
- Sample
- Maternal blood
- Expected results
- 7–12 days
About this test
A combined maternal carrier and prenatal chromosome screen with added fetal-antigen information. The catalogue describes carrier screening with conditional single-gene NIPT follow-up alongside chromosome and fetal-antigen assessments. These are screening results, not a diagnosis.
What's included
- Maternal carrier screening for selected inherited conditions, including cystic fibrosis and spinal muscular atrophy
- Single-gene NIPT reflex assessment if indicated by the carrier screen
- Screening for trisomies 13, 18 and 21 and sex chromosome differences
- Fetal sex and RhD status screening
- Selected fetal red blood cell antigen screening; confirm the exact antigen list with the clinic
- 22q11.2 deletion syndrome screening
Quick facts
- Test type: Combined carrier, aneuploidy and fetal-antigen screening
- Sample: Maternal blood
- Results: 7–12 days, with a maximum turnaround of 12 days
- Interpretation: Clinical review and confirmatory testing may be needed
Results and included services
Expected results
7–12 days
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