1. Açık Erişim@BUU
  2. İndeksli Yayınlar
  3. Web of Science
Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/24208
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dc.contributor.authorSanal, Özden-
dc.contributor.authorTezcan, İlhan-
dc.contributor.authorErsoy, Figen-
dc.date.accessioned2022-01-21T07:42:25Z-
dc.date.available2022-01-21T07:42:25Z-
dc.date.issued2002-
dc.identifier.citationKılıç, S. S. vd. (2002). "Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome". Turkish Journal of Pediatrics, 44(4), 357-359.en_US
dc.identifier.issn0041-4301-
dc.identifier.urihttp://hdl.handle.net/11452/24208-
dc.description.abstractHyperimmunoglobulin E syndrome (hyper-IgE) is a rare immunodeficiency disease associated with recurrent pyogenic infections, chronic eczematoid dermatitis and osteopenia. We present here a 13-year-old girl with hyperimmunoglobulin E syndrome, who developed osteochondritis dissecans (OCD) of the lateral femoral condyle, which is rare. Osteopenia, which is frequently associated with hyper IgE, may predispose the patient to the development of OCD.en_US
dc.language.isoenen_US
dc.publisherTürkiye Milli Pediatri Derneğitr_TR
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectBone abnormalitiesen_US
dc.subjectHyperimmunoglobulin E syndromeen_US
dc.subjectOsteochondritis dissecansen_US
dc.subjectOsteopeniaen_US
dc.subject.meshAdolescenten_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshJob's syndromeen_US
dc.subject.meshKnee jointen_US
dc.subject.meshOsteochondritis dissecansen_US
dc.titleOsteochondritis dissecans in a patient with hyperimmunoglobulin E syndromeen_US
dc.typeArticleen_US
dc.identifier.wos000179136500018tr_TR
dc.identifier.scopus2-s2.0-0036807296tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Pediatri Bölümü.tr_TR
dc.identifier.startpage357tr_TR
dc.identifier.endpage359tr_TR
dc.identifier.volume44tr_TR
dc.identifier.issue4tr_TR
dc.relation.journalTurkish Journal of Pediatricsen_US
dc.contributor.buuauthorKılıç, Sara Şebnem-
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed12458817tr_TR
dc.subject.wosPediatricsen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid34975059200tr_TR
dc.subject.scopusJob Syndrome; Mucocutaneous Candidiasis; Gain of Function Mutationen_US
dc.subject.emtreeAdolescenten_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeDermatitisen_US
dc.subject.emtreeCase reporten_US
dc.subject.emtreeDisease predispositionen_US
dc.subject.emtreeEczemaen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFemur condyleen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHyperimmunoglobulinemia Een_US
dc.subject.emtreeImmune deficiencyen_US
dc.subject.emtreeOsteochondritis dissecansen_US
dc.subject.emtreeOsteopeniaen_US
dc.subject.emtreeRecurrent infectionen_US
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