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J Pediatr ; 128(2): 285-7, 1996 Feb.
Article in English | MEDLINE | ID: mdl-8636833

ABSTRACT

Delayed response to medical treatment sometimes leads to unnecessary liver transplantation in patients with severely decompensated Wilson disease. We report the course of five patients (mean age 13.4 years, range 11 to 15 years) with severely decompensated Wilson disease who were successfully treated medically. Prothrombin time improved after a minimum of 1 month and returned to normal within 3 months to 1 year or more.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Hepatolenticular Degeneration/drug therapy , Hepatolenticular Degeneration/therapy , Penicillamine/therapeutic use , Sulfates/therapeutic use , Zinc Compounds/therapeutic use , Adolescent , Anti-Bacterial Agents/administration & dosage , Chelation Therapy , Child , Copper/urine , Female , Hemolysis , Humans , Penicillamine/administration & dosage , Prothrombin Time , Sulfates/administration & dosage , Zinc Compounds/administration & dosage , Zinc Sulfate
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