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Wilson’s disease is a rare, autosomal recessive inherited disorder characterized by excessive
copper storage, particularly in the brain, liver, kidneys, and cornea, with resultant organ dysfunction.
Five cases of Wilson’s disease were studied during the period from May 1977 to Dec. 1983
at the department of pediatrics, Yonsei University Severance hospital. The results were analyzed in relation to age and sex, family history,... |
