Wilson's disease in children
Hepatolenticular degeneration (HLD) in children is a hereditary disease of abnormal copper metabolism. It usually occurs between the ages of 10 and 25, and can occur as early as 3 years old or as late as after 50 years old. It is characterized by copper deposition in tissues such as the liver, brain, kidney, and cornea, causing a series of clinical symptoms. In recent years, great progress has been made in the research of this disease. It has been proven that this disease is completely treatable. This disease has been reported in various parts of my country, and very fruitful work has been done in early diagnosis, early treatment, and DNA analysis.
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Site of disease:
Craniocerebral Liver -
Infectious :
Not contagious -
Frequent population:
Infants and young children -
Related symptoms:
Dysarthria ataxia high fever pain in liver area ataxia -
Concurrent disease:
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