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Beschrijving
This test is primarily used in the diagnosis of Wilson’s disease, a genetic disorder characterized by copper accumulation in the liver, brain, and other tissues. It is also useful in evaluating:
- Hepatic function in relation to copper metabolism
- Menkes disease (in infants)
- Aceruloplasminemia (rare neurodegenerative disorder)
- Chronic liver disease
- Inflammatory or autoimmune conditions involving copper dysregulation
- Includes: Ceruloplasmin level measurement
- Sample requirement: Serum
Suitable for postal submission.
Additional information
Weight | 0,5 kg |
---|---|
Dimensions | 25 × 16 × 3 cm |
Sample Type |