X-linked Adrenoleukodystrophy (X-ALD) Targeted Gene Sequencing
X-linked Adrenoleukodystrophy (X-ALD) Targeted Gene Sequencing
Laboratory Fee Schedule
Procedure #
CPT: 81403
X-linked Adrenoleukodystrophy (X-ALD) Targeted Gene Sequencing
Synonym(s): | X-ALD |
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Requisition Form | G-1B (G-1B form ordering information) |
Test Description | X-linked Adrenoleukodystrophy (X-ALD) Targeted Gene Sequencing |
Pre-Approval Needed | N/A |
Supplemental Information Required | Please indicate on the requisition form the variant of interest and/or the exon you are requesting to be sequenced. |
Supplemental Form(s) | N/A |
Performed on Specimens from (sources) | Human |
Sample/Specimen Type for Testing |
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Minimum Volume/Size Required |
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Storage/Preservation Prior to Shipping | Dried filter paper blood specimens
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Transport Medium | EDTA acceptable for whole blood |
Specimen Labeling | Two patient-specific identifiers required (e.g., patient full name, date of birth, Medical record number) |
Shipping and Specimen Handling Requirements |
Ship all specimens according to Dangerous Good Regulations, IATA, and/or CFR 49. DRIED FILTER PAPER BLOOD SPECIMENS
WHOLE BLOOD SHIPPING REQUIREMENT
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Method | PCR Amplification and Sanger Sequencing |
Turn-around Time | 5 working days |
Interferences/Limitations | Pathogenic intronic variants, large deletions/duplications, or whole gene deletions/duplications may not be identified by this methodology. Molecular based testing is highly accurate. However, rare diagnostic errors may occur. Interpretation of results is dependent on the accuracy of information given to the laboratory and is limited by current technology and available X-ALD knowledge. |
Common Causes for Rejection |
Visit website for complete list. |
Additional Information | Interpretation: Available on the result report. Diagnostic Information: X-ALD DNA testing is performed in support of the Newborn Screening Program at DSHS and for other individuals. X-ALD Sanger sequencing methodology can detect approximately 97% of the known variants in this gene. Test results should not be used as a diagnostic test, but should be interpreted in the context of clinical findings, family history, and other laboratory data. Additional information for specimen collection: • View a specimen collection training video for collecting on filter paper • See Collection Tips for Venipuncture • See Instructions on how to complete a G-1B form |