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Ceruloplasmin
Measures a liver-produced protein that binds and transports copper.
Why This Biomarker Matters
Low ceruloplasmin suggests Wilson's disease, a serious genetic disorder. Early diagnosis enables copper-reducing treatment that prevents neurological and organ damage.
Optimal Ranges
Clinician-defined 4-point reference thresholds (mg/dL)
Default Range
Overview
Ceruloplasmin is a protein produced by the liver that binds and transports copper in the bloodstream. Low ceruloplasmin levels are a hallmark sign of Wilson's disease, a rare genetic disorder where copper accumulates to toxic levels in organs like the brain, liver, and eyes. Symptoms include liver disease, tremors, behavioral changes, and a characteristic golden-brown ring in the eye (Kayser-Fleischer ring). Early detection through ceruloplasmin testing is crucial because Wilson's disease is treatable with copper-reducing medications.
Technical Information (LOINC Codes)
Standardized laboratory codes for this biomarker
2064-4Primary102090-829213-646716-747600-253073-3Available Lab Tests
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