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Tests
UGT1A1*28 for Gilbert's Syndrome
A genetic test for the UGT1A1*28 polymorphism located in the promoter
region of the uridine diphosphate glucuronsyltransferase gene
- For the diagnosis of Gilbert's Syndrome
- To assess patients prior to commencing Irinotecan therapy and other
drugs metabolised by UGT1A1*28
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Test:
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UGT1A1*28
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Laboratory
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Clinical Biochemistry |
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Specimen Type:
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4 ml EDTA whole blood |
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Storage:
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4oC prior to posting
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Posting Details:
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First class mail or your chosen courier - ambient |
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Posting Address:
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Department of Clinical Biochemistry, City Hospital, Dudley
Road, Birmingham B18 7QH |
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Clinical Use:
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To help with the diagnosis of Gilbert's Syndrome.
To check patient genotype prior to treatment with Irinotecan and other drugs
that are metabolised by UGT1A1 |
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Advantages:
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Special Details:
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If you would like to send a aliquot of serum (1 ml or more) then we will
analyse liver function tests to help with our interpretation to you. |
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Turnaround:
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3 working day target |
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External QA Scheme:
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Sample sharing |
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CPA Accredited Lab/Test:
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Full |
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Cost
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£29 to NHS laboratories |
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Website:
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www.cityassays.org.uk |
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Key Contact:
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Dr Jonathan Berg |
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Clinical Lead for this assay:
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Dr Loretta Ford |
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