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dc.contributor.authorOzkavukcu, Esra
dc.contributor.authorFitoz, Suat
dc.contributor.authorYagmurlu, Banu
dc.contributor.authorCiftci, Ergin
dc.contributor.authorErden, Ilhan
dc.contributor.authorErtem, Mehmet
dc.date.accessioned2020-06-25T17:43:54Z
dc.date.available2020-06-25T17:43:54Z
dc.date.issued2007
dc.identifier.issn0301-0449
dc.identifier.urihttps://doi.org10.1007/s00247-007-0418-0
dc.identifier.urihttps://hdl.handle.net/20.500.12587/3938
dc.descriptionCiftci, Ergin/0000-0002-4955-160X; Fitoz, Suat/0000-0002-0180-0013; Ertem, Mehmet/0000-0002-8173-7885en_US
dc.descriptionWOS: 000244724900010en_US
dc.descriptionPubMed: 17297619en_US
dc.description.abstractOrbital wall infarction and subperiosteal haematomas are unusual manifestations of sickling disorders. Here we report an 11-year-old girl with sickle cell anaemia having multiple skull infarctions including the orbital bony structures associated with subperiosteal haematomas. The diagnosis was made by MRI, which showed bone marrow changes and associated haemorrhagic collections. The patient was successfully managed without surgical intervention.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.relation.isversionof10.1007/s00247-007-0418-0en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectsickle cell anaemiaen_US
dc.subjectorbiten_US
dc.subjectinfarctionen_US
dc.subjectMRIen_US
dc.subjectchilden_US
dc.titleOrbital wall infarction mimicking periorbital cellulitis in a patient with sickle cell diseaseen_US
dc.typearticleen_US
dc.identifier.volume37en_US
dc.identifier.issue4en_US
dc.identifier.startpage388en_US
dc.identifier.endpage390en_US
dc.relation.journalPediatric Radiologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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