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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.

Anisocytosis

Abnormally increased variability in the size of erythrocytes.

Total: 1

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PMID (PMCID)
21901661	FEMALE
	Atypical presentation of Wilson disease.
	Wadera S, Magid MS, McOmber M, Carpentieri D, Miloh T. Semin Liver Dis. 2011;31(3):319-26.
	Liver biopsy revealed pronounced bile ductular reaction, bridging fibrosis, and hepatocytic anisocytosis and anisonucleosis with degenerative enlarged eosinophilic hepatocytes, suggestive of Wilson disease.