Athena Diagnostics - Testing that Makes a Difference
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Periaxin DNA Sequencing Test #239
Type of Disorder: Peripheral Neuropathy
Typical Presentation: CMT with a family history of Periaxin mutations identified in a proband
Disease(s) tested for: Charcot-Marie-Tooth Disease, Type 4F (CMT4F)
Test Details
Test Code: 239
Profiles that contain this test: Complete CMT Evaluation, Complete Dejerine-Sottas Neuropathy Evaluation, Partial CMT Evaluation - Demyelinating Only, Partial CMT Evaluation - Recessive Only
Informed Consent Required: Yes
Medicare ABN Required: No
Special Notes: Use of the Complete CMT Evaluation, #390 is recommended for all new cases. When the gene is identified, a single gene test may be used for family member testing
Technical Information
Utility: Detects sequence variations in the Periaxin (PRX) gene
Methodology: Polymerase Chain Reaction (PCR) and DNA sequencing
Reference Value: No sequence variation detected
Patents: 7,273,698, 7,537,899
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(14), 83904(14), 83909(14), 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: 10ml
Collection Tube: Yellow top, ACD-A
Alternate Specimen Requirements
Type: Whole blood
Minimum Volume: 10ml
Collection Tube: lavender top (EDTA)
Storage Conditions: Room temperature, avoid freezing
Shipping Conditions: Room temperature, avoid freezing. Ship same day, must arrive Monday - Friday.
Test Turnaround: 14-21 days
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