Prenatal Holoprosencephaly Panel & Del/Dup
New York
Approved
Genes
Conditions
- Holoprosencephaly
Clinical Utility
- Full gene sequencing testing for fetuses with prenatal ultrasound findings suggestive of holoprosencephaly
- Mutation-specific testing for fetuses with a family history of a known mutation in the SHH, ZIC2, SIX3, or TGIF gene
Lab Method
- MLPA
- Next-Gen Sequencing
Test Code
2373
CPT Codes*
81479x1
ABN Required
No
Turnaround Time**
2-3 weeks
Preferred Specimen
Alternative Specimen
*The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
**Reporting times are typical and begin once the sample(s) are received at the GeneDx laboratory, but could be extended in situations outside GeneDx’s reasonable control.
Test Documents
Billing
Targeted Variant Testing