ObjectiveThe goal of the present work is to provide an overview of the differential diagnosis of Wilson disease.BackgroundWilson disease is a rare condition due to copper accumulation primarily in the liver and brain. Although there is no definitive cure, current anti-copper treatments are associated with better outcomes if initiated early and if the diagnosis is made promptly. However, diagnostic delays are frequent and often Wilson disease represents a diagnostic challenge. The diagnosis ultimately relies on a combination of clinical, laboratory and genetic findings, and it is crucial that clinicians list Wilson disease in their differential diagnosis, especially in patients presenting with a hepatocellular pattern of liver injury. Some b...
Wilson disease is an inherited, autosomal recessive, copper accumulation and toxicity disorder that ...
Wilson’s disease is an autosomal recessive disorder of copper metabolism that causes accumulation of...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Introduction. Wilson's disease represents one of the genetic diseases that has lifelong treatment, w...
Wilson's disease (WD) is a genetic metabolic disease strictly associated with liver cirrhosis. In th...
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to ...
Wilson's disease or hepatolenticular degeneration Abstract. Wilson's disease, or hepatolenticular de...
Wilson\u27s disease is a rare autosomal recessive disorder of copper metabolism that often proves a ...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Background and aim: Wilson disease (WD) is an inherited disorder ofhepatic copper excretion leading ...
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and ther...
Wilson disease (WD) is an uncommon autosomal recessive condition of impared hepatic copper excretion...
– OBJECTIVE: Wilson’s Disease (WD) is an autosomal recessive copper overload. Several mutations of t...
Wilson disease is an inherited, autosomal recessive, copper accumulation and toxicity disorder that ...
Wilson’s disease is an autosomal recessive disorder of copper metabolism that causes accumulation of...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Introduction. Wilson's disease represents one of the genetic diseases that has lifelong treatment, w...
Wilson's disease (WD) is a genetic metabolic disease strictly associated with liver cirrhosis. In th...
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to ...
Wilson's disease or hepatolenticular degeneration Abstract. Wilson's disease, or hepatolenticular de...
Wilson\u27s disease is a rare autosomal recessive disorder of copper metabolism that often proves a ...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Background and aim: Wilson disease (WD) is an inherited disorder ofhepatic copper excretion leading ...
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and ther...
Wilson disease (WD) is an uncommon autosomal recessive condition of impared hepatic copper excretion...
– OBJECTIVE: Wilson’s Disease (WD) is an autosomal recessive copper overload. Several mutations of t...
Wilson disease is an inherited, autosomal recessive, copper accumulation and toxicity disorder that ...
Wilson’s disease is an autosomal recessive disorder of copper metabolism that causes accumulation of...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...