--- Query Results --- | |||
Program: | Genetics and Genomics | ||
Test Name: | Hereditary Neuropathy with liability to Pressure Palsies (Gene: PMP22) | ||
Test Code: | CERNER: MDLBL-;APPEND TEST NAME AND SAMPLE TYPE | ||
Alternate Test Name: | HNPP | ||
Performing Site: | Alberta Children's Hospital | ||
Performing Dept: | Molecular Diagnostics | ||
TAT: | 6 - 8 weeks | ||
Preferred Tube/Container: | See Specimen Requirements | ||
Specimen Requirements: | Whole blood is the preferred specimen type for tests performed using MLPA methodology. For Blood Specimen (peripheral or cord blood) For Prenatal Specimens Submit in a sterile 15 mL or 50 mL polypropylene centrifuge tube or in a plain sterile tube with screw cap NOTE: A maternal blood sample (as outlined above) must be collected for maternal cell contamination studies. For Other Tissue Specimens placed in transport media. For Extracted DNA | ||
Min. Sample Required: | If unable to collect the minimum as per specimen requirements, contact the laboratory. | ||
Specimen Processing: | Unopened dedicated tubes (do not share) are required for Molecular Diagnostic Laboratory testing. Do not spin or aliquot specimens. For all specimen types (except frozen tissue) store specimens at ambient temperature if being shipped on same day of collection (preferred). Specimens can be stored at 4 - 8oC if shipping is delayed. Store frozen tissue specimens at -20oC to -80oC. | ||
Specimen Handling: | Transport all specimen types (except frozen tissue) at ambient temperature. Specimens must not freeze in transit. Transport frozen tissue specimens with adequate amounts of dry ice to keep specimen frozen. Specimens must not thaw in transport. Specimens, with completed requisitions, should be received by the Molecular Diagnostic Laboratory: Ship specimens to Molecular Diagnostic Laboratory at Alberta Children’s Hospital Room B0-020. | ||
Requisition/Form: | All requests MUST be submitted on a Molecular Diagnostic Laboratory Requisition. Please ensure all required information, including patient's clinical history/indication, is provided on the requisition. | ||
Order Restrictions: | Confirmation of Diagnosis1 - No restrictions Presymptomatic Testing2 - Neurology and Genetics 1 patient has signs or symptoms of the disease/disorder 2 patient does not presently have symptoms, positive family history of the condition | ||
Gene: | PMP22 | ||
Method: | MLPA and Sanger sequencing | ||
Method Details: | MLPA: Detects deletions and duplications Sanger sequencing: Analysis of all coding regions of PMP22 | ||
Reference Interval: | Interpretation provided on report. | ||
Comments: | For additional information refer to Genetic Laboratory Services webpage or contact MDL South at ACH at 403-955-7397 (phn) or 403-955-7624 (fax). | ||
Last Updated On: | Friday, September 21, 2018 | ||
Date of Last Review: | Jan 2 2018 12:00AM | ||