Wilson disease

Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.

Biliary atresia

Atresia of the biliary tree.


Total: 1

                       


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PMID (PMCID)
21453233
 MIXED_SAMPLE Child
Leukoencephalopathy syndrome after living-donor liver transplantation.
Umeda Y, Matsuda H, Sadamori H, Shinoura S, Yoshida R, Sato D, Utsumi M, Yagi T, Fujiwara T.
Exp Clin Transplant. 2011;9(2):139-44.
The underlying diseases were alcoholic cirrhosis in 3 cases, viral cirrhosis in 2, biliary atresia in 1, and Wilson disease in 1.