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SCA13 Select Exon DNA Test #284
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 13 (SCA13)
Test Details
Test Code: 284
Profiles that contain this test: Autosomal Dominant Ataxia Evaluation, Complete Ataxia Evaluation
Informed Consent Required: Yes
Medicare ABN Required: No
Special Notes: For clinical support on test ordering or result interpretation, please contact Athena's genetic counselors or lab directors. The Complete Ataxia Evaluation, #690 is recommended unless a family member's mutation has been confirmed by prior molecular tests.
Technical Information
Utility: Detects sequence variations in all of exon 2 and 20 bp of intronic sequence of the KCNC3 gene.
Methodology: Polymerase Chain Reaction (PCR) and DNA Sequencing
Reference Value: No sequence variations detected
Patents: 7,585,629
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(4), 83904(4), 83909(4), 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: 10 ml
Collection Tube: Lavender top (EDTA)
Storage Conditions: Refrigerate, avoid freezing
Shipping Conditions: Ship within 24 hours, Monday-Thursday only
Test Turnaround: 14-21 days
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