Autoimmune Axonal Neuropathy Profile
Also known as: Autoimmune Axonal Neuropathy Panel, Paraneoplastic
Use
This test should be considered for the differential evaluation of patients who present with a subacute neurological disorder of undetermined etiology, especially when nerve conduction velocity studies reveal lower amplitudes with relatively preserved conduction velocity.
Special Instructions
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or reflex tests. Testing schedules may vary.
Limitations
This test was developed and its performance characteristics determined by Labcorp in accordance with CLIA requirements. This test has not been cleared or approved by the Food and Drug Administration.
Methodology
Immunoassay (Immunofluorescence, EIA, Immunoblot)
Biomarkers
LOINC Codes
- 56850-1
- 49738-8
- 43187-4
- 43102-3
- 84924-0
- 84925-7
- 84926-5
- 33422-7
- 43103-1
- 47401-5
- 84927-3
- 82976-2
- 94347-2
- 96464-3
- 84929-9
- 84930-7
- 84931-5
- 84928-1
- 94345-6
- 82979-6
- 82978-8
Result Turnaround Time
5-7 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
2 mL
Minimum Volume
1 mL
Container
Gel barrier tube, serum transfer tube
Causes for Rejection
Gross hemolysis; grossly lipemic; gross icetrus
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 14 days |
| Refrigerated | 14 days |
| Frozen | 14 days |