Clinical Pediatrics · 1984 · 22 citations · 17 references
MedicineHematologyPediatricsClinical BiochemistryHepatologyPediatric HematologyAcute Liver FailureAnemiaHepatic PathologyLiver DiseasePediatric Liver DiseaseWilson Disease24-Hour Urinary Copper ExcretionAcute Hepatic FailureHepatic Copper MetabolismPediatric Acute Liver FailurePediatric Wilson DiseaseSerum Ceruloplasmin TestingSerum Copper MeasurementWilson Disease Differential Diagnosis
We report a child with the presentation of Wilson's disease as acute fulminant hepatic failure and severe hemolysis. Our review of the literature suggests the following criteria for considering this diagnosis in the child with acute liver failure: discordance between mildly elevated serum transaminases and extremely elevated bilirubin levels; anemia associated with hemolysis (increased reticulocytes in the absence of bleeding); elevated hepatic copper; and other copper metabolic abnormalities (elevated serum copper, excessive 24-hour urine copper excretion, and reduced serum ceruloplasmin). Establishing the correct diagnosis enhances the possibility of detecting asymptomatic siblings or other family members in whom early inauguration preventive therapy should be successful.
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Studies on Copper Metabolism. XIII. Hepatolenticular Degeneration1
G. E. Cartwright, R.E. Hodges, Clark J. Gubler et al. · Journal of Clinical Investigation · 1954 · 209 citations · Full text
Medicine, Biochemistry, Pathology +13
Wilson's disease, presenting as chronic active hepatitis
James A. Scott, John L. Gollan, S. Samourian et al. · Gastroenterology · 1978 · 136 citations · Full text
Wilson's Disease: The Presenting Symptoms
J.M. Walshe · Archives of Disease in Childhood · 1962 · 133 citations · Full text
Fulminant hepatic failure in childhood: An analysis of 31 cases
H T Psacharopoulos, A P Mowat, Melanie J. Davies et al. · Archives of Disease in Childhood · 1980 · 127 citations · Full text