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.

Chronic hepatic failure



Total: 1

                       


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PMID (PMCID)
15984949
 MALE Child
Severe hypogammaglobulinemia associated with hepatic vein stenosis causes cytomegalovirus infection after living-related liver transplantation.
Komatsu H, Inui A, Sogo T, Fujisawa T, Egawa H, Tanaka K.
Transpl Infect Dis. 2005;7(1):41-4.
An 8-year-old boy underwent living-related liver transplantation (LRLT) because of Wilson disease with chronic hepatic failure.