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.

Dyskinesia

A movement disorder which consists of effects including diminished voluntary movements and the presence of involuntary movements.


Total: 2

                       


(per page)
PMID (PMCID)
1810163
 MALE
Tongue dyskinesia as an early manifestation of Wilson disease.
Liao KK, Wang SJ, Kwan SY, Kong KW, Wu ZA.
Brain Dev. 1991;13(6):451-3.
These suggested that tongue dyskinesia could be an early sign of Wilson disease and was not the main cause of his dysarthria.
1810163
 MALE
Tongue dyskinesia as an early manifestation of Wilson disease.
Liao KK, Wang SJ, Kwan SY, Kong KW, Wu ZA.
Brain Dev. 1991;13(6):451-3.
Tongue dyskinesia as an early manifestation of Wilson disease.