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.

Healthcare professional preparing sample collection equipment beside a seated patient.
AED 5,500
Sample
Maternal blood
Expected results
7–12 days
Request an Appointment Ask on WhatsApp (opens in a new tab)
Add an appointment preference

Payment and preferred dates do not confirm an appointment. Our team will confirm collection arrangements.

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

Questions about this test

What does UNITY Complete with Fetal Antigen NIPT include? It combines carrier screening, trisomies 13, 18 and 21, sex chromosome screening, fetal RhD and selected blood-antigen information, plus 22q11.2 screening.

Is cystic fibrosis carrier screening included? The catalogue names cystic fibrosis and spinal muscular atrophy among the inherited conditions.

What sample is needed? The package lists a maternal blood sample.

When are results ready? Results are available in 7–12 days, with a maximum turnaround of 12 days.

Is this a diagnostic test? No. Screening findings should be reviewed with a clinician, who can advise on confirmatory testing.

Need help choosing a test?

Ask our team about the test and its collection instructions.

Speak with our teamAll test categories