Athena Diagnostics - Testing that Makes a Difference
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Primary Adrenal Insufficiency Evaluation #816
Type of Disorder: Adrenal
Typical Presentation: In infants: hyperpigmentation of the skin and mucosal membranes, failure to thrive, vomiting, hypoglycemia
In male children: hyperpigmentation of the skin and mucosal membranes, weakness, fatigue, orthostatic hypotension, anorexia, weight loss, nausea
Indications for Testing: Primary adrenal insufficiency in boys
Family history of X-linked adrenoleukodystrophy
Test Details
Test Code: 816
Profile includes: Autoimmune Polyglandular Syndrome (AIRE) Evaluation, ABCD1 (Adrenoleukodystrophy) DNA Sequencing Test, NR0B1 (Adrenal Hypoplasia Congenita) DNA Sequencing Test
Informed Consent Required: Yes
Medicare ABN Required: Yes
Technical Information
Utility: Detects mutations (including point mutations, deletions, insertions, and rearrangements) in the coding sequences of AIRE, NR0B1, and ABCD1 genes
Methodology: Polymerase Chain Reaction (PCR), DNA sequencing of entire protein coding region of gene
Reference Value: No mutation detected
Patents: 5,644,045, 7,217,806
CPT Coding
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.
Stacked CPT Code(s): 83891(1), 83898(31), 83904(31), 83909(31), 83912(1)
Shipping Considerations
Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form.
Preferred Specimen Requirements
Type: Whole blood
Minimum Volume: 10 mL (pediatric minimum: 2 mL)
Collection Tube: Yellow or lavender top
Stability: Hemolysis may compromise DNA recovery and integrity after 48 hrs
Storage Conditions: For short periods (until shipped) at 4°C
Shipping Conditions: Overnight at room temperature (specimen arrival must be less than 24 hrs after collection); ship Monday through Thursday only
Test Turnaround: 2 - 8 weeks
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