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dc.contributor.authorVahedi, P
dc.contributor.authorMohajernezhad, Z
dc.contributor.authorZeinali, A
dc.contributor.authorPourakbar, E
dc.date.accessioned2018-08-26T08:16:00Z
dc.date.available2018-08-26T08:16:00Z
dc.date.issued2009
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51071
dc.description.abstractFahr syndrome is known by idiopathic basal ganglia and extrabasal ganglia calcification, which is clinically manifested by movement disorders, dementia, behavioral disturbances, and cognitive impairments. The pathogenesis of this syndrome is still a matter of debate. Although abnormalities in calcium-phosphorus metabolism have been proposed as file possible etiology, no evidence is still provided. We report oil 3 patients with basal ganglia calcification without either a familial trait or hypoparathyroidism. The focus Of this paper is to illustrate extensive calcification of white and gray matter of the cerebellum in Fahr syndrome, which has not yet been reported in the literature and also to emphasize epilepsy as a rare feature of this syndrome.
dc.language.isoEnglish
dc.relation.ispartofNEUROSURGERY QUARTERLY
dc.subjectFahr's syndrome
dc.subjectbasal ganglia
dc.subjectcalcification
dc.subjectcerebellum
dc.subjectseizure
dc.titleFahr Syndrome, A Rare Neurodegenerative Disorder
dc.typeArticle
dc.citation.volume19
dc.citation.issue1
dc.citation.spage69
dc.citation.epage71
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1097/WNQ.0b013e31818d19aa


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