Athena Diagnostics - Testing that Makes a Difference
Test Catalog
SearchBrowse

Enter symptom, disease type, test name or code


SearchBrowse

Use this pull down menu to view all tests offered within a disorder cateogy.

Test Catalog

SCA6 DNA Test #373
Type of Disorder: Movement Disorders
Typical Presentation: Ataxia, poor coordination of hand, speech and eye movements, uncoordinated and unsteady gait
Disease(s) tested for: Spinocerebellar ataxia type 6 (SCA6)
Test Details
Test Code: 373
Profiles that contain this test: Autosomal Dominant Ataxia Evaluation, Complete Ataxia Evaluation
Informed Consent Required: Yes
Medicare ABN Required: Yes
Special Notes: The Complete Ataxia Evaluation, #690 is recommended unless a family member's mutation has been confirmed by prior molecular tests.
Technical Information
Utility: Detects CAG triplet repeat expansion in the SCA6 gene
Methodology: Polymerase Chain Reaction (PCR) and Fragment Analysis by Capillary Electrophoresis
Reference Value: Normal: < 18 CAG trinucleotide repeats
Patents: 5,853,995, 6,303,307, 7,329,487
CPT Coding
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.
Stacked CPT Code(s): 83891(1), 83898(1), 83909(1), 83912(1)
Shipping Considerations
Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form.
Preferred Specimen Requirements
Type: Whole blood
Minimum Volume: 20ml
Collection Tube: Lavender top (EDTA)
Storage Conditions: Refrigerate, avoid freezing
Shipping Conditions: Room temperature, avoid freezing. Ship within 24 hours, Monday - Thursday only.
Test Turnaround: 7-14 days
Canada US