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General
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Clinical Use:
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The determination of oxalate in urine is important for the diagnosis and treatment of both oxalate kidney stone disease and the rare condition of primary hyperoxaluria. Type 1 primary hyperoxaluria is due to reduced activity of alphaketoglutarate:glyoxylate carboligase, and is characterised by increased urinary glycolate. Type 2 hyperoxaluria is due to the absence of D-glyceric acid dehydrogenase, and is accompanied by increased urinary L-glycerate.
Increases in oxalate excretion are also associated with pyridoxine deficiency, and with chronic ileal disease. |
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Availability:
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Samples are batched and tested once a week.
This test can only be performed on patients >=7 years of age.
If a 24hr urine is received on a patient <7 years of age, please register as a spot urine sample (UOXCR). |
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Code:
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24OX |
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Handling Instructions (to laboratory):
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Send sample chilled. |
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Hyperlink:
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Reference Interval:
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Male:
7 years to <15 years: 140-420 mmol/day
15 years to <120 years: 80-490 mmol/day
Female:
7 years to <15 years: 140-420 mmol/day
15 years to <120 years: 40-340 mmol/day
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Collection Requirements
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Container:
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UR24 Sulphamic Acid (UR24SULP), |
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Sample Type:
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See container |
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Minimum Collection Volume:
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10mL |
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Collection Instructions:
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Processing Requirements
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Alternate Containers:
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Processing Instructions:
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Refer to local manual for processing requirements. |
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Minimum Assay Volume:
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10mL |
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Stability:
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Transport Instructions (to testing laboratory):
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Send sample chilled. |
Testing Locations
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Performed at:
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Section
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Department
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Site
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Contact Phone
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| Special Chemistry |
Biochemistry |
Fiona Stanley Hospital |
6152 2830 |
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Last Updated : 13-08-2025 13:19 |