Wilson Disease Panel Test
Test Cost: AED 940.0
Symptoms, Diagnosis, and Referring Details:
Test Name: Wilson Disease Panel Test
Test Components:
- CBC
- LFT
- Ceruloplasmin
- Copper, Serum
- Copper, 24-hour Urine
Price: 940.0 AED
Sample Condition:
- 3 mL (1 mL min.) whole blood in 1 Lavender Top (EDTA) tube
- 2 mL (1.5 mL min.) serum from 1 SST
- 3 mL (1.0 mL min.) serum from 1 metal free White top(Z- No additive) tube available from LPL
- 10 mL (5 mL min.) aliquot of 24-hour urine collected in an acid washed (metal free) container available from LPL
Ship refrigerated. DO NOT FREEZE. Use powderless gloves during specimen collection.
Report Delivery: Sample Mon through Sat by 6 pm; Report Next day
Method: Spectrophotometry, Nephelometry, Electrical Impedence, VCS, ICPMS
Test Type: Disorders of Liver
Doctor: Physician, Gastroenterologist, Opthalmologist
Test Department:
Pre Test Information: If Barium containing contrast media has been administered, the specimen should not be collected for 96 hours.
Test Details:
The Wilson disease panel test is a diagnostic tool used to identify and confirm the presence of Wilson disease, which is a genetic disorder that causes copper to accumulate in the body’s tissues, particularly the liver and brain.
The panel typically includes several tests:
- Ceruloplasmin: This test measures the levels of ceruloplasmin, a protein that helps transport copper in the blood. Low levels of ceruloplasmin are often indicative of Wilson disease.
- Copper: This test measures the amount of copper in the blood. Elevated copper levels may suggest Wilson disease.
- 24-hour urine copper: This test measures the amount of copper excreted in the urine over a 24-hour period. High levels of copper in the urine can be a sign of Wilson disease.
- Liver function tests: These tests assess the overall function of the liver, which is often affected by Wilson disease. Abnormal liver function may indicate the presence of the condition.
- Genetic testing: Genetic testing can identify mutations in the ATP7B gene, which is responsible for the production of a protein involved in copper transport. Mutations in this gene are associated with Wilson disease.
By analyzing the results of these tests, healthcare providers can make a definitive diagnosis of Wilson disease and determine the appropriate treatment plan. Treatment typically involves medications to reduce copper levels and dietary changes to limit copper intake.
| Test Name | WILSON DISEASE PANEL Test |
|---|---|
| Components | *CBC *LFT *Ceruloplasmin*Copper, Serum *Copper, 24 hour Urine |
| Price | 940.0 AED |
| Sample Condition | 3 mL (1 mL min.) whole blood in 1 Lavender Top (EDTA) tube AND 2 mL (1.5 mL min.) serum from 1 SST AND 3 mL (1.0 mL min.) serum from 1 metal free White top(Z- No additive) tube available from LPL AND 10 mL (5 mL min.) aliquot of 24 hour urine collected in an acid washed (metal free) container available from LPL. Ship refrigerated. DO NOT FREEZE. Use powderless gloves during specimen collection. |
| Report Delivery | SampleMon through Sat by 6 pm ;Report Next day |
| Method | Spectrophotometry,Nephelometry, Electrical Impedence, VCS,ICPMS |
| Test type | Disorders of Liver |
| Doctor | Physician, Gastroenterologist, Opthalmologist |
| Test Department: | |
| Pre Test Information | If Barium containing contrast media has been administered, the specimen should not be collected for 96 hours. |
| Test Details | The Wilson disease panel test is a diagnostic tool used to identify and confirm the presence of Wilson disease, which is a genetic disorder that causes copper to accumulate in the body’s tissues, particularly the liver and brain. The panel typically includes several tests: 1. Ceruloplasmin: This test measures the levels of ceruloplasmin, a protein that helps transport copper in the blood. Low levels of ceruloplasmin are often indicative of Wilson disease. 2. Copper: This test measures the amount of copper in the blood. Elevated copper levels may suggest Wilson disease. 3. 24-hour urine copper: This test measures the amount of copper excreted in the urine over a 24-hour period. High levels of copper in the urine can be a sign of Wilson disease. 4. Liver function tests: These tests assess the overall function of the liver, which is often affected by Wilson disease. Abnormal liver function may indicate the presence of the condition. 5. Genetic testing: Genetic testing can identify mutations in the ATP7B gene, which is responsible for the production of a protein involved in copper transport. Mutations in this gene are associated with Wilson disease. By analyzing the results of these tests, healthcare providers can make a definitive diagnosis of Wilson disease and determine the appropriate treatment plan. Treatment typically involves medications to reduce copper levels and dietary changes to limit copper intake. |
