Sensory Neuropathy Antibody Panel with Reflex to Titer and Neuronal Immunoblot
Also known as: SNAP R
Use
This test aids in diagnosing sensory neuropathy in patients where malignancy is suspected, excluding plasma cell dyscrasia. It includes detection of antibodies such as SGPG IgM, MAG IgM, and Purkinje Cell/Neuronal Nuclear IgG. Positive results could indicate active demyelination in peripheral neuropathy or paraneoplastic neurological disorders associated with certain cancers.
Special Instructions
The test is carried out in a CLIA certified laboratory and is intended for clinical purposes. Additional charges apply if reflex tests are performed due to positive initial outcomes.
Limitations
This test has not been cleared or approved by the US Food and Drug Administration. Its performance characteristics were determined by ARUP Laboratories. The test is intended strictly for clinical purposes; results must be interpreted in the context of patient's overall clinical picture.
New York Approved
Methodology
Immunoassay (ELISA)
Biomarkers
LOINC Codes
- 17314-6
- 31666-1
- 61177-2
Result Turnaround Time
2-9 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
2 mL
Minimum Volume
1 mL
Container
ARUP Standard Transport Tube
Collection Instructions
Separate serum from cells ASAP or within 2 hours of collection.
Causes for Rejection
Other body fluids. Contaminated, heat-inactivated, hemolyzed, grossly icteric, or lipemic specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 24 hours |
| Refrigerated | 2 weeks |
| Frozen | 1 year |
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