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Wilson Disease Panel Test

940 د.إ

-10%

The Wilson Disease Panel Test is a comprehensive diagnostic tool used to detect Wilson Disease, a rare genetic disorder that leads to excessive accumulation of copper in the body’s tissues, causing neurological, psychiatric, and liver-related symptoms. This panel test primarily focuses on identifying mutations in the ATP7B gene, which are indicative of Wilson Disease. Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services, the test costs 940 AED. Through a simple blood sample, the test aims to provide accurate genetic information, enabling early diagnosis and appropriate management of the condition. DNA Labs UAE ensures confidentiality and precision in their testing processes, making it a reliable choice for individuals seeking clarity on their genetic predisposition to Wilson Disease.

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  • This test is not intended for medical diagnosis or treatment
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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:

  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.

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.