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Congenital ocular motor apraxia

dc.contributor.authorCarrasquinho, S
dc.contributor.authorTeixeira, S
dc.contributor.authorCadete, A
dc.contributor.authorBernardo, M
dc.contributor.authorPêgo, P
dc.contributor.authorPrieto, I
dc.date.accessioned2012-11-13T16:50:56Z
dc.date.available2012-11-13T16:50:56Z
dc.date.issued2008
dc.description.abstractPURPOSE: Congenital ocular motor apraxia is a rare disease characterized by defective or absent voluntary and optically induced horizontal saccadic movements. Jerky head movements or thrusts on attempted lateral gaze are a compensatory sign. Most affected children have delayed motor and speech development. Cases associated with systemic diseases, neurologic maldevelopment, metabolic deficits, and chromosomal abnormalities have been described. METHODS: Case report and review of the scientific literature. RESULTS: The authors describe the ophthalmologic, pediatric, and neurologic evaluations and follow up of a child with impaired horizontal saccades, jerky head movements, and delayed motor and speech development. CONCLUSIONS: Congenital ocular motor apraxia is an uncommon disorder of ocular motility. Even so, ophthalmologists should be aware of the developmental delay and the other associated conditions, in order to grant the patients the multidisciplinary assistance they often require.por
dc.identifier.citationEur J Ophthalmol. 2008 Mar-Apr;18(2):282-4por
dc.identifier.issn1120-6721
dc.identifier.urihttp://hdl.handle.net/10400.10/750
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherWichtig Editorepor
dc.subjectPerturbações da motilidade ocularpor
dc.subjectCriançapor
dc.subjectPerturbações do desenvolvimentopor
dc.titleCongenital ocular motor apraxiapor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceMilãopor
oaire.citation.endPage284por
oaire.citation.startPage282por
oaire.citation.titleEuropean journal of ophthalmologypor
oaire.citation.volume18por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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