TITLE

Ocular motility and Wilson's disease: a study on 34 patients

AUTHOR(S)
Ingster-Moati, I.; Quoc, E. Bui; Pless, M.; Djomby, R.; Orssaud, C.; Guichard, J. P; Woimant, F.
PUB. DATE
November 2007
SOURCE
Journal of Neurology, Neurosurgery & Psychiatry;Nov2007, Vol. 78 Issue 11, p1199
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Background: Wilson's disease is an autosomal recessive genetic disorder resulting from an abnormality of copper metabolism. The excessive accumulation of copper in the brain induces an extrapyramidal syndrome. Oculomotor abnormalities occur in most extrapyramidal disorders but have rarely been studied in Wilson's disease. Objective: To evaluate the ocular motility manifestations of Wilson's disease. Methods: A prospective study of 34 patients affected by Wilson's disease who were recruited and their ocular motility recorded by electro-oculography (EOG). Results: Vertical smooth pursuit was abnormal in 29 patients (85%). Vertical optokinetic nystagmus and horizontal smooth pursuit were impaired in 41% and 41% of patients, respectively. No MRI abnormality was found in the lenticular nuclei of seven patients who manifested ocular motility abnormalities. Conclusion: Vertical eye movements, in particular vertical pursuits, are impaired in Wilson's disease, more often than vertical optokinetic nystagmus and vertical saccades. EOG abnormalities can be found in patients who do not yet exhibit anatomical lesions on MRI.
ACCESSION #
27560538

 

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