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Original Article
Two Cases of Wilson's Disease.
Dae Young Kim, In Kwyn Park, jong Sik Kim, Kang Ho Kim, Sang Kee Park, Chang Soo Ra
Clin Exp Pediatr. 1987;30(12):1475-1479.   Published online December 31, 1987
Two cases of Wilson’s disease were experienced, which showed symptoms of hepatic dysfunction, Kayser-Fleischer ring and decreased serum ceruloplasmin and increased urine copper excretion. Case 1: An 9 years old boy was admitted with abdominal distension and general edema, he had low serum ceruloplasmin levels (7.0 mg%) and high levels of urinary copper (2020 必g/24 hrs) and increased transaminase levels (292 U/L of SGOT,...
A Case of Wilson's Disease.
Hee Joo Jeon, Yong Joon Kim, Hi Joo Park, Chan Yung Kim, Jong Woo Shin
Clin Exp Pediatr. 1987;30(2):201-206.   Published online February 28, 1987
Department of Pediatrics, College of Medicine, Pusan National University Wilson’s disease is due to excessive accumulation of copper in the liver, brain, kidneys and cornea caused by a defect in biliary excretion. The classic presentation of Wilson’s disease is the triad of neurologic abnormalities, Kayser- Fleischer ring and cirrhosis associated with low serum copper and ceruloplasmin levels. The case, 12-year-old boy, suffered from jaundice, abdominal...
Case Report
Two Cases of Wilson's Disease.
Myung Ho Kang, Byoung Tae Kim, Jae Ock Park, Sang Jhoo Lee
Clin Exp Pediatr. 1986;29(3):336-341.   Published online March 31, 1986
The authors experienced two cases of hepatic from of Wilson* s disease, which diagnosis were confirmed by family history, their characteristic clinical manifestations with hepatic symptoms, Kayser-Fleischer ring and laboratory data with decreased serum ceruloplasmin and copper level and increased urine copper excretion. Case 1： An 8 8/12 year-old boy with chief complaints of abdominal distension and jaundice showed Kayser-Fleischer ring...
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