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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 liver problems, unusual neurological symptoms like tremors or difficulty with coordination, or mood and behavioral changes that don't have a clear cause. It helps identify Wilson's disease, a rare genetic condition where copper builds up in your liver, brain, and other organs, causing serious damage if left untreated. This test is especially important if you have a family history of Wilson's disease or if your doctor suspects copper metabolism problems.
No special preparation is typically required for this test, though you should inform your doctor if you're taking any copper supplements or medications that might affect copper metabolism. It's best to take this test when you're not acutely ill, as infections and inflammation can temporarily affect ceruloplasmin levels. Follow any specific instructions provided by your healthcare provider, and make sure to stay well-hydrated before your blood draw.
This panel evaluates copper metabolism by measuring ceruloplasmin (the protein that carries copper in your blood) and serum copper levels. Together, these measurements help identify whether your body is retaining too much copper, which can damage your liver, brain, kidneys, and eyes. Low ceruloplasmin combined with abnormal copper levels is a key indicator of Wilson's disease and helps guide further diagnostic steps.
What this means
Your ceruloplasmin level is below the normal range, which is one of the key indicators of Wilson's disease when combined with other copper metabolism markers. Low ceruloplasmin means your body isn't producing enough of this protein that carries copper in your blood, potentially leading to copper accumulation in organs. This finding warrants follow-up testing and consultation with a specialist to confirm diagnosis and begin appropriate treatment.
Recommended actions
Consult with a hepatologist or genetic specialist for comprehensive Wilson's disease evaluation
Consider additional testing including 24-hour urine copper and slit-lamp eye exam
Begin discussing copper-restricted diet options with your healthcare provider
Have family members screened if Wilson's disease is confirmed
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