Glucose 6 Phosphate Dehydrogenase (G6PD) deficiency screen Directory Icon  - Kings Pathology Printer Icon - Kings Pathology

Haematology Overview / Directory

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Purpose of the test

Description: G6PD deficiency is a common hereditary enzyme deficiency causing varying degrees of haemolytic anemia; can cause favism, some drug induced haemolytic anemias, and chronic nonspherocytic haemolytic anemia. Any samples with a deficient screen will have a full G6PD assay performed.

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Reference Range

End point up to 60 minutes

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Sample Requirements

Minimum 1 ml EDTA blood. FBC and reticulocyte count must be performed and results sent with samples. Samples with a reticulocyte count > 2.0% will require a G6PD assay performed. If more than one enzyme assay is required then > 1.0 ml of blood will be required.

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Storage and Transport

Samples can be sent first class post. Samples must be received in the laboratory within 3 days of collection. If there is a delay in sending store at 4°C

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Turnaround Time

10 working days

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Time Limit for Extra Tests

Depends on tests required. Contact laboratory for further details.

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Factors affecting results or interpretation

Recent blood transfusion.

Raised reticulocyte levels and/or raised WBC levels may affect assay.

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Contacts

Tel 020 3299 9000 Laboratory Ext 2455 Office Ext 4337

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