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.

Congenital hepatic fibrosis

The presence of fibrosis of that part of the liver with congenital onset.


Total: 1

                       


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PMID (PMCID)
19207220
 MIXED_SAMPLE Child
New-onset diabetes mellitus presenting with diabetic ketoacidosis after pediatric liver transplantation.
Dehghani SM, Nikeghbalian S, Eshraghian A, Haghighat M, Imanieh MH, Bahador A, Kazemi K, Malek-Hosseini SA.
Pediatr Transplant. 2009;13(5):536-9.
The underlying diseases leading to transplantation were cryptogenic liver cirrhosis, Wilson disease, and congenital hepatic fibrosis.