What is Wilson disease? Wilson disease is an inherited condition that causes the body to retain excess copper. The liver of a person who has Wilson's disease does not ...
What is Wilson Disease? Wilson disease (WD) is a rare inherited disorder of copper metabolism in which excessive amounts of copper accumulate in the body.
Wilson's disease — Comprehensive overview covers symptoms, causes, treatment of this copper metabolism disorder.
Wilson disease is a genetic disorder that is fatal unless detected and treated before serious illness from copper poisoning develops. Wilson disease affects ...
Wilson's disease also called Wilson disease or hepatolenticular degeneration is an autosomal recessive genetic disorder in which copper accumulates in tissues; this ...
Wilson disease is a rare autosomal recessive inherited disorder of copper metabolism that is characterized by excessive deposition of copper in the liver ...
Wilson's disease is an autosomal recessive disorder of copper metabolism. Despite being treatable, there is no universally accepted treatment regimen.
Symptoms of Wilson's Disease including 84 medical symptoms and signs of Wilson's Disease, alternative diagnoses, misdiagnosis, and correct diagnosis for Wilson's ...
Important It is possible that the main title of the report Wilson's Disease is not the name you expected. Please check the synonyms listing to find the ...
Describes the cause, symptoms, and diagnosis of Wilson disease and summarizes treatment options.