Wilson’s disease is a rare genetic disorder characterized by excessive accumulation of copper in vital organs such as in the liver and the brain. If left untreated, this condition can lead to liver disease and critical dysfunctions in the nervous system.
Getting tested for the levels of copper in your body will provide substantial information on the therapy and nutritional supplementation of copper to those who are diagnosed with Wilson’s disease. Despite being a rare hereditary disorder, Wilson’s disease can be treated when diagnosed early.
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