21 HYDROXYLASE COMMON MUTATION
Synonyms: | CAH, Common Mutations; 21 Hydroxylase Deficiency; Congenital Adrenal Hyperplasia; CYP21A2 |
Computer Code: | (N21HY) |
Specimen Collection: | 5 mL blood (lavender top tube). Royal blue EDTA Yellow ACD Genetic consent required (See Test Requisitions and Consents #6) |
Minimum Volume: | 3 mL |
Handling Instructions for Offsite Areas: | Maintain whole blood at room temperature. Min 3 mL whole blood. |
Reference Values: | See reference laboratory report. |
Lab Code: | Send Out |
Requisition: | SPEC C |
Test Frequency: | NA |
Routine TAT: | 14 days |
Stat TAT: | N/A |
CPT Code(s): | 81402 |
LCD or NCD: | |
Methodology Used: |
See Addendum XVII |