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

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dc.authorid0000-0002-8440-367X
dc.contributor.authorBayram, Merve
dc.contributor.authorYıldırım, Mine
dc.contributor.authorSeymen, Figen
dc.date.accessioned10.07.201910:49:13
dc.date.accessioned2019-07-10T19:52:21Z
dc.date.available10.07.201910:49:13
dc.date.available2019-07-10T19:52:21Z
dc.date.issued2015
dc.departmentİstanbul Medipol Üniversitesi, Diş Hekimliği Fakültesi, Çocuk Diş Hekimliği Ana Bilim Dalı
dc.descriptionWOS: 000214141500010
dc.descriptionPubMed ID: 25245233
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. Case report This patient had supernumerary nipples on the right side, cubitus valgus webbed fingers, scoliosis, umbilical hernia, a coarse face, macrocephaly, hypertelorism, a short broad nose, a wide mouth, a straight facial profile and hearing loss. The patient also had macroglossia, diastemas, over-retained primary tooth, absent mandibular permanent central incisors, and highly arched palate. Lateral cephalometric analysis revealed a large anterior cranial base, a large maxilla and mandible, a large inferior face height, and skeletal Class III jaw relationship. Follow-up After extraction of the over-retained primary central tooth, a partial prosthesis was fabricated in order to maintain function. The patient has been recalled regularly at 6-month intervals for 2 years. Over the following years the prosthesis was replaced due to facial growth. Conclusion Long term follow-up is essential for the patient with SGBS. Preventive dental care, including oral hygiene instructions, diet counselling and the use of fluoride has been implemented.
dc.identifier.citationBayram, M., Yıldırım, M. ve Seymen, F. (2015). Clinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome. European Archives of Paediatric Dentistry, 16(1), 63-66. https://dx.doi.org/10.1007/s40368-014-0141-0
dc.identifier.doi10.1007/s40368-014-0141-0
dc.identifier.endpage66
dc.identifier.issn1818-6300
dc.identifier.issn1996-9805
dc.identifier.issue1
dc.identifier.scopusqualityQ2
dc.identifier.startpage63
dc.identifier.urihttps://dx.doi.org/10.1007/s40368-014-0141-0
dc.identifier.urihttps://hdl.handle.net/20.500.12511/2386
dc.identifier.volume16
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofEuropean Archives of Paediatric Dentistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectSimpson-Golabi-Behmel Syndrome
dc.subjectOvergrowth Syndrome
dc.subjectOral Findings
dc.titleClinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome
dc.typeArticle

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