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.

Hepatic failure



Total: 2

                       


(per page)
PMID (PMCID)
29540233
(5853083)
 MIXED_SAMPLE Adult
Novel compound heterozygote mutations inthe ATP7B gene in an Iranian family with Wilson disease: a case report.
Daneshjoo O, Garshasbi M.
J Med Case Rep. 2018;12(1):68.
Hepatic failure and neuronal degeneration are the major symptoms of Wilson disease.
25380954
 FEMALE Adult
Pregnancy in a patient with hepatic artery thrombosis after liver transplantation: a case report.
Tronina O, Mikolajczyk N, Pietrzak B, Pacholczyk M, Durlik M.
Transplant Proc. 2014;46(8):2929-31.
We describe a case of a 30-year-old woman with hepatic failure owing to Wilson disease.