Clinical and demographic features of pediatric-onset Behcet's disease and evaluation of optical coherence tomography findings

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dc.authorid0000-0003-4468-3985
dc.authorid0000-0003-0645-8170
dc.contributor.authorBalbaba, Mehmet
dc.contributor.authorUlaş, Fatih
dc.contributor.authorPostacı, Sevinç Arzu
dc.contributor.authorÇeliker, Ülkü
dc.contributor.authorGürgöze, Metin Kaya
dc.date.accessioned2021-06-23T19:55:01Z
dc.date.available2021-06-23T19:55:01Z
dc.date.issued2020
dc.departmentBAİBÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.description.abstractPurpose: To evaluate the clinical characteristics, including spectral domain optical coherence tomography (SD-OCT) findings, of pediatric-onset Behcet's disease (PBD) patients. Methods: Medical records of 23 PBD (15 males and 8 females) and 24 (15 males and 9 females) healthy subjects were evaluated retrospectively. The main outcomes were compared between PBD patients, with and without ocular involvement, and healthy subjects. Results: The mean age at onset was 12.00 +/- 2.10 years. Mean follow-up period was 25.17 +/- 15.36 months (range 6-48). Retinal vasculitis was the most common ocular finding (7 patients). Most of the complications of systemic treatment were associated with long term corticosteroid therapy. There was no significant difference between the mean retinal thickness of the PBD patients and healthy controls (p > 0.05). The mean choroidal thickness was significantly increased in all measured segments of PBD patients with ocular involvement (p < 0.01). Conclusion: Choroidal thickness of PBD patients with ocular involvement was significantly thicker compared to the PBD patients without ocular involvement and to healthy control subjects.en_US
dc.identifier.doi10.1080/09273948.2019.1611875
dc.identifier.endpage612en_US
dc.identifier.issn0927-3948
dc.identifier.issn1744-5078
dc.identifier.issue4en_US
dc.identifier.pmid31560571en_US
dc.identifier.scopus2-s2.0-85073924168en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage606en_US
dc.identifier.urihttps://doi.org/10.1080/09273948.2019.1611875
dc.identifier.urihttps://hdl.handle.net/20.500.12491/10708
dc.identifier.volume28en_US
dc.identifier.wosWOS:000487908200001en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.institutionauthorUlaş, Fatih
dc.language.isoenen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofOcular Immunology And Inflammationen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBehcet's Diseaseen_US
dc.subjectChoroidal Thicknessen_US
dc.subjectOptical Coherence Tomographyen_US
dc.subjectPediatric-onset Behcet's Diseaseen_US
dc.subjectRetinal Thicknessen_US
dc.titleClinical and demographic features of pediatric-onset Behcet's disease and evaluation of optical coherence tomography findingsen_US
dc.typeArticleen_US

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