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Test Identifier Information

 
Registration CodeAGGD
Method

The DNA sample is analysed for HBA gene copy number using a multiplex ligatable probe (MLPA) based assay (MRC-Holland) followed by detection/quantification on an ABI3130xl genetic analyser.

Diagnostic Use / Indications

The alpha thalassemias are a group of genetic disorder characterized by the absence or reduction of alpha globin chain synthesis. This results in varying degrees of microcytic and hypochromic anaemia. Alpha thalassaemia may be caused by the deletion of one or both copies of the alpha-globin genes, HBA1 and HBA2, on chromosome 16p13.3 and can result in mild to severe anaemia. Specific deletions are commonly found in individuals of Mediterranean, Middle Eastern, South East Asian and Polynesian origin.

Constituent TestsGenomic DNA Extraction ;
External Price$250.00(Exclusive of GST)
  

Specimen Collection

 
Pre-Testing Requirements

 MLPA based assays are sensitive to the buffer used in DNA extraction processes. Due to this, our preference is to recieve whole blood (EDTA) which will then be extracted at Canterbury Health Laboratories. Processing of DNA extracted at other centers may result in a request for a new sample if the analysis is compromised.

Patient Specimen4.0mL EDTA,
Paediatric Specimen0.5 mL - 1 mL EDTA blood
Sample Delivery to LabSame day or overnight courier, ambient
  

CHLabs Laboratory

 
DepartmentBiochemistry - Molecular Pathology
Contact Details Email Email
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Contact Phone Number03 3640 548
Test Availability9am to 5pm, Monday to Friday
Turnaround TimeWithin 4 weeks
Additional Information
  1. This test requires nucleated cells. Please do not centrifuge or freeze blood samples.
  2. Genomic DNA must be extracted from the specimen prior to testing. This incurs an additional charge (see GDNA). 
Delphic Number Test Number3154

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