The copper metabolism disorder Wilson's disease was first defined in 1912. Wilson's
disease can present with hepatic and neurological deficits, including dystonia and …

Wilson disease is one of the few movement disorders in which there are therapies that
modify disease progression. This disease is caused by copper overload primarily in the liver …

Copper is an essential metal required for many metalloproteins' function. A fraction of dietary
copper (average 2–5 mg/day) is absorbed by enterocytes in the duodenum and proximal …

This Clinical Practice Guideline (CPG) has been developed to assist physicians and other
healthcare providers in the diagnosis and management of patients with Wilson's disease …

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

Clinical practice guidelines for Wilson's disease (WD) have been published by the American
Association for the Study of Liver Diseases and European Association for the Study of the …

Wilson disease is a rare, inherited autosomal recessive disease of copper metabolism and
may be more common where consanguinity is prevalent. Much has been known about the …

Neurologic symptoms in Wilson disease (WD) appear at an older age compared to hepatic
symptoms and manifest in patients with misdiagnosed liver disease, in patients when the …

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 …

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 …