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.

Focal dystonia

A type of dystonia that is localized to a specific part of the body.

Total: 2

(per page)

PMID (PMCID)
24166573	MALE	Young Adult
	Acute focal dystonia induced by a tricyclic antidepressant in a patient with Wilson disease: a case report.
	Litwin T, Chabik G, Czlonkowska A. Neurol Neurochir Pol. 2013;47(5):502-6.
	Acute focal dystonia induced by a tricyclic antidepressant in a patient with Wilson disease: a case report.
24166573	MALE	Young Adult
	Acute focal dystonia induced by a tricyclic antidepressant in a patient with Wilson disease: a case report.
	Litwin T, Chabik G, Czlonkowska A. Neurol Neurochir Pol. 2013;47(5):502-6.
	The authors present the case of a 19-year-old patient with Wilson disease (WD) who developed symptoms of acute focal dystonia of the left hand (a 'starfish' hand presentation) shortly after treatment with the tricyclic antidepressant clomipramine.