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Go directly to the lab, no extra fees
With friendly doctor's notes & guidance
Lab visit as quick as 10 mins in & out
We stand behind our service
Go directly to the lab, no extra fees
With friendly doctor's notes & guidance
Lab visit as quick as 10 mins in & out
This test is ideal if you're experiencing unexplained neurological symptoms like tremors, difficulty speaking, or movement problems, or if you have signs of liver disease without a clear cause. It helps diagnose Wilson's disease, a rare genetic condition where copper builds up in your body and damages your liver and brain. Many people use this test when they have a family history of Wilson's disease or when doctors need to investigate abnormal liver function.
No special preparation is typically required for this test. You can eat and drink normally before your blood draw, and you don't need to adjust your medications unless your doctor specifically instructs you otherwise. Simply schedule your appointment at a convenient time.
This test measures ceruloplasmin, a protein made by your liver that carries copper throughout your body. Low levels can indicate Wilson's disease, where copper accumulates in organs and causes damage, while high levels may suggest liver inflammation or other conditions. This single biomarker provides crucial insights into copper metabolism disorders and certain liver diseases.
What this means
Your ceruloplasmin level is below the optimal range, which may indicate a copper metabolism disorder such as Wilson's disease. Low ceruloplasmin can lead to copper accumulation in the liver and brain, potentially causing liver damage and neurological symptoms. This result warrants follow-up testing to measure copper levels directly and evaluate your liver function.
Recommended actions
Follow up with your doctor for additional copper testing and liver function evaluation
Avoid copper-rich foods like shellfish, nuts, chocolate, and mushrooms until you consult your healthcare provider
Keep track of any symptoms like tremors, mood changes, or signs of jaundice
Consider genetic counseling if Wilson's disease is confirmed, as family members may need screening