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.

Arthropathy



Total: 3

                       


(per page)
PMID (PMCID)
21654009
 MALE Child
Reversal of severe Wilson arthropathy by liver transplantation.
Nagral A, Sathe K.
Indian Pediatr. 2011;48(5):406-7.
We describe a patient of Wilson disease with severe arthropathy, which completely reversed following liver transplantation.
21654009
 MALE Child
Reversal of severe Wilson arthropathy by liver transplantation.
Nagral A, Sathe K.
Indian Pediatr. 2011;48(5):406-7.
This is the first case report in literature describing the complete reversal of Wilson disease related arthropathy by liver transplantation.
15459818
 MALE Adult
Subchondral cyst of the tibia secondary to Wilson disease.
Kataoka M, Tsumura H, Itonaga I, Kaku N, Torisu T.
Clin Rheumatol. 2004;23(5):460-3.
These findings may contribute to our better comprehension of the development process of the arthropathy in patients with Wilson disease.