Wilson’s disease is an autosomal recessive disorder affecting copper transport; it results in the accumulation of copper in the liver, brain, and other organs. Wilson’s disease is the most common inherited liver disease with more than 500 cases reported in Korea. An impairment in biliary excretion process leads to copper accumulation in the liver, which progressively damages the liver, leading to cirrhosis. Since effective treatment is available for this disease, early and correct diagnosis is very important. Here, we report a case of Wilson’s disease with mildly elevated liver enzyme levels in a 29-year-old breast-feeding woman with weight loss
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to ...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
Wilson’s disease is an autosomal recessive disorder of copper metabolism that causes accumulation of...
Wilson’s disease is a rare autosomal recessive disorder characterized by accumulation of copper in t...
Wilson’s disease is a rare, inherited autosomal recessive disease of copper metabolism, in which the...
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...
Wilson’s disease (WD), also known as hepatolenticular degeneration, is an autosomal recessive inheri...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
ABSTRACTWilsons disease is an inherited autosomal genetic abnormality genetic abnormality which resu...
Wilson’s disease (WD) is a rare autosomal recessive disorder of hepatocellular copper deposition. Th...
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and ther...
Wilson’s disease is a rare inherited disorder and is characterized by the accumulation of copper in ...
Wilson disease is an inherited, autosomal recessive, copper accumulation and toxicity disorder that ...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to ...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
Wilson’s disease is an autosomal recessive disorder of copper metabolism that causes accumulation of...
Wilson’s disease is a rare autosomal recessive disorder characterized by accumulation of copper in t...
Wilson’s disease is a rare, inherited autosomal recessive disease of copper metabolism, in which the...
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...
Wilson’s disease (WD), also known as hepatolenticular degeneration, is an autosomal recessive inheri...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
ABSTRACTWilsons disease is an inherited autosomal genetic abnormality genetic abnormality which resu...
Wilson’s disease (WD) is a rare autosomal recessive disorder of hepatocellular copper deposition. Th...
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and ther...
Wilson’s disease is a rare inherited disorder and is characterized by the accumulation of copper in ...
Wilson disease is an inherited, autosomal recessive, copper accumulation and toxicity disorder that ...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to ...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
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