Athena Diagnostics - Testing that Makes a Difference
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MEN2 (RET) Evaluation #813
Type of Disorder: Family Cancer Syndromes
Typical Presentation: MEN2A and FMTC: Neck mass or pain, diarrhea, MEN2B: diarrhea or constipation, neuromas on distal surface of tongue, mucosal surface of upper eyelids, vermillion border of lips, marfanoid habitus
Indications for Testing: Medullary thyroid cancer; Pheochromocytoma; Family history of MEN2
Disease(s) tested for: Multiple Endocrine Neoplasia Type 2, Familial Medullary Thyroid Cancer, Pheochromocytoma
Test Details
Test Code: 813
Profiles that contain this test: Pheochromocytoma Evaluation
Informed Consent Required: Yes
Medicare ABN Required: Yes
Technical Information
Utility: Detects mutations in the coding sequence of RET
Methodology: Polymerase Chain Reaction (PCR), DNA sequencing of entire protein coding region of the RET gene
Reference Value: No mutation detected
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(20), 83904(20), 83909(20), 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: Lavender top (EDTA) or yellow top (ACD-A)
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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