Virilization Panel 2
Ordering Recommendation
Aids in the detection of nonclassical congenital adrenal hyperplasia in individuals presenting with hyperandrogenism.
New York DOH Approval Status
Specimen Required
Collect between 6-10 a.m.
Serum separator tube or green (sodium or lithium heparin). Also acceptable: Pink (K2EDTA).
Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 1.2 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.7 mL)
Refrigerated.
Ambient: 24 hours; Refrigerated: 1 week; Frozen: 6 months
Methodology
Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry
Performed
Sun-Sat
Reported
1-5 days
Reference Interval
Test Number |
Components |
Reference Interval |
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Testosterone by Mass Spec |
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17-Hydroxyprogesterone, HPLC-MS/MS |
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Androstenedione by TMS |
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Dehydroepiandrosterone by TMS |
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Interpretive Data
Free or bioavailable testosterone measurements may provide supportive information.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
Note
Hotline History
Hotline History
CPT Codes
82157; 83498; 84403; 82626
Components
Component Test Code* | Component Chart Name | LOINC |
---|---|---|
0081058 | Testosterone by Mass Spec | 2986-8 |
0092332 | 17-Hydroxyprogesterone, HPLC-MS/MS | 1668-3 |
2001639 | Androstenedione by TMS | 1854-9 |
2001641 | Dehydroepiandrosterone by TMS | 2193-1 |
Aliases
- 17-Hydroxyprogesterone (Virilization Panel 2)
- Androstenedione (Virilization Panel 2)
- Dehydroepiandrosterone (Virilization Panel 2)
- Testosterone (Virilization Panel 2)