Ambiguous Genitalia Panel
Use
The Ambiguous Genitalia Panel is designed for individuals with relevant clinical features suggestive of differences or disorders in sex development. It targets patients with ambiguous or abnormal external genitalia to assist with diagnosing these complex conditions.
Special Instructions
To order the test, please ensure using the appropriate test requisition form, which includes all necessary patient, specimen, and billing information. The test can be processed using standard institutional pricing after signing in.
Limitations
The results from the Ambiguous Genitalia Panel should be interpreted within the context of a comprehensive clinical assessment. This panel may not detect all genetic variations associated with sex developmental disorders, and potential variants of unknown significance may require further investigation.
New York Approved
Methodology
NGS (CGP)
Biomarkers
Result Turnaround Time
14-21 days
Related Documents
For more information, please review the documents below
Specimen
Whole Blood
Volume
Not provided
Minimum Volume
Not provided