Corrected: Wilson’s Disease: A Prevalence Study in a Portuguese Population This article has
been corrected. Page 1 Review began 07/27/2023 Review ended 08/12/2023 Published …

Objectives: Wilson's disease is an autosomal recessive disorder that affects copper
metabolism leading to copper accumulation in the liver, nervous system, and cornea. There …

Wilson's disease first described by Kinnier Wilson in 1912, is a rare autosomal recessive
genetic disorder involving a defect in copper metabolism. This disease affects between one …

Wilson's disease is an autosomal recessive disease resulting in defective copper
metabolism, which is usually seen in young adults, predominantly affecting liver and brain …

WilsonГs disease, an inborn error of copper metabolism, is a relatively rare familial disorder
inherited as an autosomal recessive trait but treatable condition that often presents …

Wilson's disease is an autosomal recessive inherited disorder of copper metabolism
resulting in accumulation of copper in various tissues. The hallmarks of the disease are the …

Wilson's disease belongs to the group of hereditary diseases for which pathogenetic therapy
has been developed, which allows, with timely initiation of treatment, to avoid the severe …

Background & Aims The clinical prevalence of Wilson's disease (WD) in the UK remains
unknown. The estimated genetic prevalence in the UK, 142/million, is higher than the clinical …

Wilson's disease, the most common inherited disorder of copper metabolism, is a recessive
genetic condition. The clinical presentation of Wilson's disease is very variable. It is …

Background Wilson disease (WD) is an autosomal recessive disorder of hepatic copper
excretion. About sixty per cent of patients present with liver disease. WD is considered a fatal …