| Test code: | 660 |
| Type of disorder: | Peripheral Neuropathy, Hereditary |
| Disease(s) tested for: | Hereditary Sensory and Autonomic Neuropathy (HSAN) |
| Genes Included: |
ATL1, |
| Informed Consent Required: | This test requires physician attestation that patient consent has been received |
| Clinical Significance: | Detects sequence variants in the ATL1 gene
Typical Presentation: Symptom onset in the second decade of life or later. Prominent early sensory loss and lancinating pain, variable distal motor involvement, and no visceral signs of autonomic involvement.
Indications for testing: Patients presenting with Prominent early sensory loss and lancinating pain, variable distal motor involvement, and no visceral signs of autonomic involvement. in the second decade of life or later. |
| Methodology: |
Sanger Sequencing
|
| Reference Range: | No sequence variants detected |
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.
Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form.
| Specimen Type: | Whole blood |
| Specimen Stability: |
Room temperature: 10 days, Refrigerated: 10 days, Frozen: Unacceptable, |
| Specimen Requirements: |
8 mL (6 mL minimum) whole blood collected in two (lavender-top) EDTA tubes. Pediatric (0-3 years): 2 mL (1 mL minimum) |
| Instructions: | Higher blood volumes ensure adequate DNA quantity, which varies with WBC, specimen condition, and need for confirmatory testing. Patients, 0-3 years have higher WBC, yielding more DNA per mL of blood |
| Transport Temperature: | Room temperature |
| Set-up/Analytic Time: | 14-28 days |
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