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Updated: Aug 21, 2025

Positron Emission Tomography Using 64-Copper as a Tracer for the Study of Copper-Related Disorders
Published on: April 28, 2023
Black liver in a patient with Wilson's disease
Wei Jiang1, Qingmin Zeng1, Chang-Hai Liu1
1Center of Infectious Diseases West China Hospital of Sichuan University Chengdu China.
Abstract:
Wilson's disease is an autosomal recessive inherited disease with congenital copper metabolism disorder, characterized by decreased ceruloplasmin and increased urine copper, which can involve multiple organs. This case was complicated by iron overload, which is of great value in differentiating hereditary hemochromatism.
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