Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

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.

Premature osteoarthritis

Total: 2

(per page)

PMID (PMCID)
29381936 (5708935)	MALE	Adult
	Genotype and clinical course in 2 Chinese Han siblings with Wilson disease presenting with isolated disabling premature osteoarthritis: A case report.
	Ye S, Dai T, Leng B, Tang L, Jin L, Cao L. Medicine (Baltimore). 2017;96(47):e8641.
	Premature osteoarthritis (POA) is a rare condition in Wilson disease (WD).
29381936 (5708935)	MALE	Adult
	Genotype and clinical course in 2 Chinese Han siblings with Wilson disease presenting with isolated disabling premature osteoarthritis: A case report.
	Ye S, Dai T, Leng B, Tang L, Jin L, Cao L. Medicine (Baltimore). 2017;96(47):e8641.
	Genotype and clinical course in 2 Chinese Han siblings with Wilson disease presenting with isolated disabling premature osteoarthritis: A case report.