Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
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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.

Dysphagia

Difficulty in swallowing.

Total: 1

(per page)

PMID (PMCID)
22261259	MIXED_SAMPLE
	[Diagnosis and care of Wilson disease with neurological revelation].
	Wagner S, Brunet AS, Bost M, Lachaux A, Broussolle E, Des Portes V, Lion-Francois L. Arch Pediatr. 2012;19(3):271-6.
	Neurologic symptoms are present in 35% of the patients with Wilson disease such as dystonia, extrapyramidal syndrome, dysarthria, dysphagia, and psychiatric symptoms.