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Complete Alport Syndrome Evaluation #759
Type of Disorder: Kidney Disorders, Alport Syndrome
Typical Presentation: Hematuria, proteinuria and progressive renal failure, often leading to bilateral sensorineural hearing loss and ocular defects
Disease(s) tested for: Alport Syndrome
Test Details
Test Code: 759
Profile includes: COL4A3 DNA Sequencing Test, COL4A4 DNA Sequencing Test, COL4A5 Sequencing and Deletion Analysis
Informed Consent Required: Yes
Medicare ABN Required: Yes
Technical Information
Utility: Detects mutations in the COL4A3, 4, 5 genes and deletions in COL4A5
Methodology: DNA sequencing, Multiplex Ligation-dependent Probe Amplification
Reference Value: No sequence variation or deletion 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(151), 83900(1), 83901(69), 83904(99), 83909(153), 83912(1), 83914(71)
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: 15 mL
Collection Tube: Lavender top (EDTA)
Stability: Hemolysis may compromise DNA recovery and integrity after 48 hrs
Storage Conditions: Room temperature, avoid freezing
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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