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Clinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome

dc.contributor.authorBayram, M.
dc.contributor.authorSeymen, F.
dc.contributor.authorYildirim, M.
dc.date.accessioned2021-03-02T21:02:27Z
dc.date.available2021-03-02T21:02:27Z
dc.date.issued2015
dc.identifier.citationBayram M., Yildirim M., Seymen F., "Clinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome", EUROPEAN ARCHIVES OF PAEDIATRIC DENTISTRY, cilt.16, sa.1, ss.63-66, 2015
dc.identifier.othervv_1032021
dc.identifier.otherav_051a1761-1f9b-444d-9f74-5449d938be3c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/9311
dc.identifier.urihttps://doi.org/10.1007/s40368-014-0141-0
dc.description.abstractBackground The Simpson-Golabi-Behmel syndrome (SGBS) is an overgrowth condition characterised by macrosomia, mental deficiency, large head, prominent skull sutures, midface deficiency, hypertelorism, broad nose, wide mouth, macroglossia, malocclusion, highly arched palate, and musculoskeletal and limb abnormalities. The aim of this case report is to present clinical and oral findings of an 8-year-old boy who had been diagnosed with SGBS.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDiş Hekimliği
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectDİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP
dc.titleClinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome
dc.typeMakale
dc.relation.journalEUROPEAN ARCHIVES OF PAEDIATRIC DENTISTRY
dc.contributor.departmentİstanbul Medipol Üniversitesi , ,
dc.identifier.volume16
dc.identifier.issue1
dc.identifier.startpage63
dc.identifier.endpage66
dc.contributor.firstauthorID220953


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