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.

Acute hepatitis

Short-term infection iwith one of the five hepatitis viruses that causes inflammation of the liver.

Total: 1

(per page)

PMID (PMCID)
20422502	FEMALE	Young Adult
	A patient with persistent pruritus.
	Liu LU, Qin L, Knisely AS. Semin Liver Dis. 2010;30(2):205-9.
	Laboratory and radiology test results eliminated the possibility of acute hepatitis A/B/C viral infections, primary biliary cirrhosis, autoimmune hepatitis, Wilson disease, paraneoplastic cholestasis, and obstructive biliary disease.