Autoimmune Dementia Profile

Create a Free Account to View Prices

Turnaround Time: 5-7 Days
CPT Code:

86255 x18; 86341

Test Type: 2 mL Serum


Use: This test should be considered for the differential evaluation of patients who present with rapidly progressive dementia of undetermined etiology, especially with cognitive impairment and neuronal degeneration.

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; Immunofluorescence, EIA, Immunoblot

Collection Details:

Collection Instructions:

Specimen: Serum (gel barrier tube or red-top tube)

Volume: 2 mL

Minimum Volume: 1 mL

Container: Gel barrier tube, serum transfer tube

Stability Requirements: Room Temperature