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SELECTED SCENARIO · 04
Ongoing pregnancy or prenatal indication
Time-sensitive fetal exome, array, or familial-variant testing.
Clinical test selectorStep 2 of 4
- ✓Clinical scenario
- 2Diagnostic objective
- 3Available material
- 4Recommendation
STEP 2
What must the test help answer?
Select the primary diagnostic objective. Alternatives will be shown after the material check.
Ultrasound finding or broad fetal question
Fetal–parent ExomeXtra with inheritance and CNV analysis.
A chromosome deletion or duplication is suspected
Prenatal genome-wide array CGH.
A familial gene or variant is already known
Targeted prenatal confirmation may be most efficient.
No ultrasound finding, but severe early-onset risk is the question
A specialist-reviewed >2,000-gene prenatal filter can be considered.
Cannot define one primary objective?
For complex phenotypes, conflicting previous results, or unclear tumor questions, begin with a case review instead of forcing a selection.
Prepare a case enquiry →