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Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia

dc.contributor.authorBarzegar, M
dc.contributor.authorSayadnasiri, M
dc.contributor.authorTabrizi, A
dc.date.accessioned2018-08-26T08:53:56Z
dc.date.available2018-08-26T08:53:56Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54046
dc.description.abstractOculodentodigitalis dysplasia (ODDD) is an extremely rare inherited disorder involving the development of the face, eyes, teeth and limbs. In addition, some patients develop neurological problems mostly a spastic paraparesis associated with white matter abnormalities on magnetic resonance imaging. This report describes a patient with epilepsy, a rare neurologic manifestation of this syndrome.
dc.language.isoEnglish
dc.relation.ispartofIranian Journal of Child Neurology
dc.subjectbaclofen
dc.subjectbilirubin
dc.subjectcarbamazepine
dc.subjectphenobarbital
dc.subjectphenytoin
dc.subjecttimolol
dc.subjectanteverted nostril
dc.subjectarticle
dc.subjectbilirubin blood level
dc.subjectcamptodactyly
dc.subjectcase report
dc.subjectchild
dc.subjectclinical feature
dc.subjectdysplasia
dc.subjectelectroencephalogram
dc.subjectepilepsy
dc.subjectepileptic state
dc.subjectgait
dc.subjectgait disorder
dc.subjectgenetic disorder
dc.subjectglaucoma
dc.subjecthuman
dc.subjecthyperbilirubinemia
dc.subjecthypoplasia
dc.subjectmacrogyria
dc.subjectmale
dc.subjectmicrophthalmia
dc.subjectneurologic examination
dc.subjectnuclear magnetic resonance imaging
dc.subjectoculodentodigitalis dysplasia
dc.subjectphototherapy
dc.subjectphysical examination
dc.subjectphysiotherapy
dc.subjectschool child
dc.subjectspastic paraplegia
dc.subjectspasticity
dc.subjecttonic clonic seizure
dc.subjectvisual acuity
dc.titleEpilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia
dc.typeArticle
dc.citation.volume6
dc.citation.issue3
dc.citation.spage39
dc.citation.epage43
dc.citation.indexScopus


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