Copper poisoning of the body due to a rare genetic degenerative disease of the liver (hepatolenticular degeneration) is known as Wilson's disease. Failure of the liver to filter and remove excess copper leads to copper build-up in other organs. It can be life-threatening to leave it untreated. Copper accumulation causes varied symptoms based on the organ affected. Kayser-Fleischer rings or K-F rings are golden or brown ringed discoloration in the eye is common in such patients. Chelating therapies to remove excess copper from the body and oral Zinc tablets to keep the body from absorbing copper are the treatment modalities.
Renal Involvement in Wilson Disease: An Overview
Wilson disease can lead to renal tubular dysfunction and disrupt the kidneys' capacity to regulate copper homeostasis.
Wilson’s Disease in Children: Genetic Diagnosis and Long-Term Management
Wilson disease is a copper accumulation disorder affecting children with hepatic and neurological manifestations. Early detection is essential.
Trientine: Uses, Dosage, Safety, and More.
Trientine is a chelating drug used to treat Wilson's disease, a rare illness that causes copper buildup in organs.
Zinc Acetate Treatment for Wilson's Disease: A Lifesaving Approach
Wilson's illness is treated with Zinc acetate, which encourages the production of metallothionein protein, aiding in the removal of excess copper from the body.
Wilson Disease - Causes, Symptoms, and Treatment
Wilson disease is a rare genetically inherited disorder with excessive deposition of copper in the body. Its symptoms and treatment are listed in the article.

Hepatic Copper Overload Syndrome - Clinical Features and Management
Hepatic copper overload syndrome occurs due to the body's inability to excrete excess copper from the body. Read the article to know more.