Wilson disease is a genetic disorder of the liver characterized by excess accumulation of
copper, which is found ubiquitously on earth and normally enters the human body in small …

Current and Emerging Issues in Wilson’s Disease | New England Journal of Medicine Skip to
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Wilson disease (WD) is an inherited disorder of chronic copper toxicosis characterized by
excessive copper deposition in the body, primarily in the liver and the brain. It is a …

Wilson's disease (WD), also known as hepatolenticular degeneration, is an autosomal
recessive inherited disorder resulting from abnormal copper metabolism. Reduced copper …

Iron and copper ions play important roles in many physiological functions of our body, even
though the exact mechanisms regulating their absorption, distribution and excretion are not …

Wilson disease (WD) is a rare disorder of copper metabolism that presents mainly with
hepatic and neuropsychiatric features. Copper accumulates not only in the liver and brain …

Wilson's disease (WD) is a rare autosomal recessive disorder of hepatocellular copper
deposition. The diagnostic approach to patients with WD may be challenging and is based …

The redox activity of copper is of vital importance for biochemical and bioenergetic cellular
homeostasis. However, cellular copper overload leads to cell death. Wilson disease patients …

Wilson's disease (WD) is characterised by a deleterious accumulation of copper in the liver
and brain. It is one of those rare genetic disorders that benefits from effective and lifelong …

Wilson disease is a disorder of copper metabolism that, when untreated, can present with
hepatic, neurologic, or psychiatric disturbances–or a combination of these–in individuals …