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.

Cognitive impairment

Abnormality in the process of thought including the ability to process information.


Total: 1

                       


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PMID (PMCID)
11445646
 MALE Child
A 13-year-old boy with cognitive impairment, retinoblastoma, and Wilson disease.
Riley D, Wiznitzer M, Schwartz S, Zinn AB.
Neurology. 2001;57(1):141-3.
A 13-year-old boy with cognitive impairment, retinoblastoma, and Wilson disease.