Forms and Documents
- Identification of the specific molecular basis of holoprosencephaly and microform variants
- Genetic counseling, carrier testing, and recurrence risk assessment
- Preparation for prenatal testing in future pregnancies
*Reporting times are typical, but could be extended in situations outside GeneDx's reasonable control.
**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.