UNITY Carrier Screen


Price: AED 2,300.00

Sample: Maternal blood

Results: 10-15 Days

Overview

UNITY Carrier Screen assesses whether the mother carries selected inherited-condition variants. The catalogue also describes a single-gene NIPT (sgNIPT) follow-up when a carrier finding calls for it. A clinician can explain the scope and any next steps.


What's included

• Maternal carrier screening for selected inherited conditions
• Cystic fibrosis and spinal muscular atrophy among the conditions named in the catalogue
• Additional inherited-disease screening; confirm the complete condition list with the clinic
• sgNIPT assessment of the baby's DNA when the mother is identified as a carrier, as described in the source
• BabyPeek is available free of charge as an add-on to UNITY packages.


FAQ

What is the UNITY Carrier Screen?

It screens the mother for selected inherited conditions and describes conditional sgNIPT follow-up if a carrier finding is identified.

Which conditions are named?

The catalogue mentions cystic fibrosis and spinal muscular atrophy, plus other inherited diseases. Confirm the complete condition list with the clinic.

What sample is needed?

The catalogue specifies a maternal blood sample.

Does every patient receive sgNIPT follow-up?

The source describes assessment of the baby's DNA if the mother is found to be a carrier. Confirm eligibility and scope with the clinic.

When are results available?

Confirm this package's specific turnaround with the clinic before booking.

Conditions related

Symptoms related

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