Introduction Wilson's disease (WD) is a treatable genetic disorder caused by impaired
copper metabolism. Early diagnosis and correct anti-copper treatment are crucial for …

Background: The progression of Wilson disease (WD), a disorder of copper metabolism, can
be arrested by chelation therapy. However, neurologic deficits may persist despite adequate …

BACKGROUND AND PURPOSE: Neurologic Wilson disease is an inherited disease
characterized by a copper metabolic disorder that causes damage to many organs …

BACKGROUND: Wilson disease patients present with any of several neurologic
phenotypes, and their treated outcomes vary widely. Our goal was to determine whether …

Abstract Introduction Wilson's Disease (WD) is an autosomal recessive disorder caused by
excessive copper deposition in liver, brain and other organs. The clinical picture is …

Wilson's disease (WD) is a genetic disorder of copper metabolism with pathological copper
accumulation in many organs, resulting in clinical symptoms, mostly hepatic and …

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 an inherited disorder of copper metabolism, resulting in
pathological accumulation of copper, principally in the liver, brain and cornea. The causative …

Background & aims Wilson's disease (WD) is a genetic disorder of copper metabolism
causing dysfunctions of various organs, mostly the liver and brain. If untreated, WD is fatal …

Introduction Brain magnetic resonance imaging (MRI) studies on Wilson's disease (WD)
show lack of correlations between neurological and neuroimaging features. Long-term …