Wilson's disease (WD) is a rare autosomal recessive disorder of copper metabolism resulting in copper-induced tissue damage that primarily involves the liver and central nervous system. The neurologic manifestations of WD almost universally involve a derangement of basal ganglia function or psychiatric disturbance. We report the case of a 46-year-old man presenting with end-stage liver disease caused by WD who had associated rapidly progressive optic neuropathy. We also discuss the possible association between the two conditions
Wilson's disease (WD) is an autosomal recessive disorder characterized by copper overload. In this d...
Wilson's disease is a rare autosomal recessive disorder of copper metabolism. The main features refl...
Wilson's disease or hepatolenticular degeneration Abstract. Wilson's disease, or hepatolenticular de...
Wilson's disease (WD) is a rare autosomal recessive disorder of copper metabolism resulting in coppe...
Wilson’s disease (WD), also known as hepatolenticular degeneration, is a rare autosomal recessive co...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
Wilson disease (WD) is an uncommon recessive genetic disorder affecting copper metabolism. Cardiac,...
Kayser-Fleischer ring is the well known ocular manifestation of Wilson's disease (WD), which is a ra...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson's disease (WD) is an autosomal recessive disorder with reduced biliary excretion of copper pl...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Aim: Wilson's disease (WD) is a hereditary disease that causes the accumulation of copper in many or...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Wilson's disease (WD) is an autosomal recessive disorder characterized by copper overload. In this d...
Wilson's disease (WD) is an autosomal recessive disorder characterized by copper overload. In this d...
Wilson's disease is a rare autosomal recessive disorder of copper metabolism. The main features refl...
Wilson's disease or hepatolenticular degeneration Abstract. Wilson's disease, or hepatolenticular de...
Wilson's disease (WD) is a rare autosomal recessive disorder of copper metabolism resulting in coppe...
Wilson’s disease (WD), also known as hepatolenticular degeneration, is a rare autosomal recessive co...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
Wilson disease (WD) is an uncommon recessive genetic disorder affecting copper metabolism. Cardiac,...
Kayser-Fleischer ring is the well known ocular manifestation of Wilson's disease (WD), which is a ra...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson's disease (WD) is an autosomal recessive disorder with reduced biliary excretion of copper pl...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Aim: Wilson's disease (WD) is a hereditary disease that causes the accumulation of copper in many or...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Wilson's disease (WD) is an autosomal recessive disorder characterized by copper overload. In this d...
Wilson's disease (WD) is an autosomal recessive disorder characterized by copper overload. In this d...
Wilson's disease is a rare autosomal recessive disorder of copper metabolism. The main features refl...
Wilson's disease or hepatolenticular degeneration Abstract. Wilson's disease, or hepatolenticular de...