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HSP, Common Dominant Evaluation
Test Code93078
CPT Codes
81405 (x2), 81406 (x2), 81479<br><strong>CPT coding may differ dependent on payer rules which may impact prior authorization testing.</strong><br><strong>Please direct any questions regarding CPT coding to the payer being billed.</strong><br><br><strong>This test is not available for New York patient testing.</strong><br>Limited Access Code
Preferred Specimen
8 mL whole blood collected in two EDTA (lavender-top) tubes
Pediatric (0-3 years): 2 mL whole blood
Pediatric (0-3 years): 2 mL whole blood
Minimum Volume
6 mL • Pediatric: 1 mL
Transport Temperature
Room temperature
Specimen Stability
Room temperature: 10 days
Refrigerated: 10 days
Frozen: Unacceptable
Refrigerated: 10 days
Frozen: Unacceptable
Methodology
Next Generation Sequencing
Setup Schedule
Set up: Varies; Report available: 28-42 days
Reference Range
See Laboratory Report
Clinical Significance
This test includes sequencing 4 genes including: ATL1, SPAST, REEP1, KIF5A, and a SPAST deletion test. This test will detect 70-80% of genetic causes of autosomal dominant HSP.

