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.

Thoracic kyphosis

Over curvature of the thoracic region, leading to a round back or if sever to a hump.

Total: 1

(per page)

PMID (PMCID)
25252715 (4177382)	FEMALE	Child
	Congential scoliosis in Wilson's disease: case report and review of the literature.
	Li Z, Yu X, Shen J, Liang J. BMC Surg. 2014;14:71.
	This study is to present a case of thoracic kyphosis occurring in the setting of Wilson'disease and explore the possible association between the two diseases.