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 …

Wilson's disease is an autosomal-recessive disorder of copper metabolism with hepatic,
neurological, psychiatric, ophthalmological, haematological, renal, and rheumatological …

Wilson disease, or hepatolenticular degeneration, is a rare autosomal recessive disorder
resulting from mutations in the ATP7B gene on chromosome 13, leading to defective copper …

Wilson's disease (WD) is a hereditary disorder of copper metabolism, producing abnormally
high levels of non-ceruloplasmin-bound copper, the determinant of the pathogenic process …

Malnutrition and sarcopenia are common in patients with chronic liver disease and are
associated with increased risk of decompensation, infections, wait-list mortality and poorer …

Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the
liver and secondly in other organs, such as the central nervous system. It is a hereditary …

Recent studies have expanded the phenotype of Wilson disease, identified rare inherited
metal-related disorders that resemble Wilson disease, and studied long-term outcomes of …

Wilson's disease (WD) is an uncommon hereditary disorder caused by a deficiency in the
ATP7B transporter. The protein codified by this gene facilitates the incorporation of the …

Wilson's disease is an autosomal-recessive disorder of copper metabolism with neurological
and hepatic presentations. Chelation therapy is used to 'de-copper'patients but neurological …

Wilson's disease (WD) is a rare, autosomal recessive disorder of copper metabolism caused
by pathogenic mutations in the ATP7B gene. Cellular copper overload is associated with …