Athena Diagnostics - Testing that Makes a Difference
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Friedreich Ataxia DNA Test #119
Type of Disorder: Movement Disorders
Typical Presentation: Ataxia, poor coordination of hand, speech and eye movements, uncoordinated and unsteady gait
Disease(s) tested for: Friedreich's ataxia
Test Details
Test Code: 119
Profiles that contain this test: Complete Ataxia Evaluation, Friedreich's Ataxia Profile
Informed Consent Required: Yes
Medicare ABN Required: No
Special Notes: The Complete Ataxia Evaluation (#597) is recommended unless a family member has been confirmed by prior molecular tests. Prenatal testing is available for this test.
Technical Information
Utility: Detects GAA triplet repeat expansion in the Frataxin gene
Methodology: Polymerase Chain Reaction (PCR), Fragment analysis and Southern blot
Reference Value: Normal: < 33 GAA trinucleotide repeats
Patents: 6,150,091
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), 83894(1), 83898(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: 14-21 days
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