CERULOPLASMIN

The ceruloplasmin test measures the level of ceruloplasmin, a copper-carrying protein, in the blood. This test is used to diagnose Wilson’s disease, a rare genetic disorder that causes excessive copper accumulation in the body. Low levels of ceruloplasmin can indicate Wilson’s disease, leading to copper buildup in the liver, brain, and other organs. The test is valuable for diagnosing and monitoring Wilson’s disease, guiding treatment decisions, and assessing the effectiveness of therapy. It provides important information for managing copper metabolism disorders and preventing complications associated with copper toxicity.