Your browser doesn't support javascript.
loading
Severely decompensated abdominal Wilson disease treated with peritoneal dialysis: a case report.
Kuno, T; Hitomi, T; Zaitu, M; Sato, T; Yoshida, N; Miyazaki, S.
Affiliation
  • Kuno T; Department of Pediatrics, Saga Medical School, Nabeshima, Japan. kuno@post.saga-med.ac.jp
Acta Paediatr Jpn ; 40(1): 85-7, 1998 Feb.
Article in En | MEDLINE | ID: mdl-9583209
A 12-year-old girl with severely decompensated abdominal Wilson disease was treated with abdominal dialysis in order to accelerate the excretion of chelated copper. Dialysate without human serum albumin or D-penicillamine was used and was able to accelerate the excretion of chelated copper, with an increment of 5.5-19.7% compared with urinary excretion only.
Subject(s)
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Peritoneal Dialysis / Hepatolenticular Degeneration Limits: Child / Female / Humans Language: En Journal: Acta Paediatr Jpn Year: 1998 Document type: Article Affiliation country: Japan Country of publication: Australia
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Peritoneal Dialysis / Hepatolenticular Degeneration Limits: Child / Female / Humans Language: En Journal: Acta Paediatr Jpn Year: 1998 Document type: Article Affiliation country: Japan Country of publication: Australia