The Ceruloplasmin test is a laboratory test used to measure the levels of ceruloplasmin in the blood. Ceruloplasmin is a protein synthesized in the liver and plays an essential role in copper metabolism. The test is primarily performed to evaluate the function and levels of ceruloplasmin in the body.
Wilson's Disease: Wilson's disease is a genetic disorder characterized by impaired copper metabolism, leading to the accumulation of copper in various organs, particularly the liver, brain, and eyes. A Ceruloplasmin test is often used as an initial screening test for Wilson's disease. Low levels of ceruloplasmin are commonly seen in individuals with this condition.
Copper Deficiency: In cases of suspected copper deficiency, a Ceruloplasmin test may be ordered to assess the levels of ceruloplasmin. Copper deficiency can occur due to malabsorption, inadequate dietary intake, or certain medical conditions. Low levels of ceruloplasmin may indicate copper deficiency.
The Ceruloplasmin Test is a simple blood test that can be performed in a laboratory. Before the test, the patient may be asked to avoid certain medications that may affect the results. During the test, our healthcare professional will use a needle to draw blood from a vein in the patient's arm. The blood sample will then be sent to our laboratory for analysis.
Interpreting Ceruloplasmin test results involves comparing the measured levels of ceruloplasmin with established reference ranges. Low levels of ceruloplasmin may indicate conditions such as Wilson's disease or copper deficiency, while high levels may suggest inflammation or other underlying medical conditions.
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