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dc.contributor.authorGlass, Lora R. Dagi
dc.contributor.authorDagi, Teodoro Forcht
dc.contributor.authorDagi, Linda
dc.date.accessioned2013-02-15T18:49:07Z
dc.date.issued2011
dc.identifier.citationGlass, Lora R. Dagi, Teodoro Forcht Dagi, and Linda R. Dagi. 2011. Papilledema in the setting of X-linked hypophosphatemic rickets with craniosynostosis. Case Reports in Ophthalmology 2(3): 376-381.en_US
dc.identifier.issn1663-2699en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:10304389
dc.description.abstractPurpose: Introduction to the ophthalmic literature of an unusual cause of papilledema and subsequent optic atrophy: X-linked hypophosphatemic rickets (XLH). Methods: Case report of a 3-year-old female presenting with papilledema resulting from craniosynostosis secondary to XLH. Results: Early intervention with craniofacial surgery prevented the development of optic atrophy. Conclusion: Children with XLH should be screened for ophthalmic evidence of elevated intracranial pressure to aid early intervention and prevention of permanent loss of vision.en_US
dc.language.isoen_USen_US
dc.publisherS. Karger AGen_US
dc.relation.isversionofdoi:10.1159/000334941en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250662/pdf/en_US
dash.licenseLAA
dc.subjectpapilledemaen_US
dc.subjectoptic atrophyen_US
dc.subjectricketsen_US
dc.subjectcraniosynostosisen_US
dc.titlePapilledema in the Setting of X-Linked Hypophosphatemic Rickets with Craniosynostosisen_US
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden_US
dc.relation.journalCase Reports in Ophthalmologyen_US
dash.depositing.authorDagi, Linda
dc.date.available2013-02-15T18:49:07Z
dc.identifier.doi10.1159/000334941*
dash.authorsorderedfalse
dash.contributor.affiliatedDagi, Linda
dash.contributor.affiliatedDagi, Teodoro Forcht


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