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.

Anemia

A reduction in erythrocytes volume or hemoglobin concentration.


Total: 1

                       


(per page)
PMID (PMCID)
21757830
 MALE Adult
Excess copper chelating therapy for Wilson disease induces anemia and liver dysfunction.
Harada M, Miyagawa K, Honma Y, Hiura M, Shibata M, Matsuhashi T, Abe S, Harada R, Tabaru A.
Intern Med. 2011;50(14):1461-4.
Excess copper chelating therapy for Wilson disease induces anemia and liver dysfunction.