Inherited Platelet Function Disorder Panel
Use
This test is intended for individuals with relevant clinical features who have a clinically suspected or confirmed diagnosis of inherited platelet function disorders. It aims to identify genetic variants across 26 genes associated with these disorders, providing valuable insights for diagnosis and potential management strategies.
Special Instructions
For accurate results, ensure specimen collection and shipping are handled properly. The test can be ordered through myPrevent or by faxing in the requisition form with necessary information filled out. STAT testing is available with an additional charge, and institutional standard pricing applies upon signing in.
Limitations
This panel is designed to detect specific genetic variants known to be associated with inherited platelet function disorders. However, it may not detect all genetic abnormalities involved in these conditions. The test's sensitivity and specificity are subject to the quality of the sample and coverage depth. Genes with insufficient coverage may yield inconclusive results, and rare genetic mutations may not be detected.
New York Approved
Methodology
NGS (Targeted)
Biomarkers
Result Turnaround Time
14-21 days
Related Documents
For more information, please review the documents below
Specimen
Whole Blood
Volume
Not provided
Minimum Volume
Not provided