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

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Atıf İçin Kopyala

Bayram M., Yildirim M., Seymen F.

EUROPEAN ARCHIVES OF PAEDIATRIC DENTISTRY, cilt.16, sa.1, ss.63-66, 2015 (ESCI)

• Yayın Türü: Makale / Tam Makale
• Cilt numarası: 16 Sayı: 1
• Basım Tarihi: 2015
• Doi Numarası: 10.1007/s40368-014-0141-0
• Dergi Adı: EUROPEAN ARCHIVES OF PAEDIATRIC DENTISTRY
• Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus
• Sayfa Sayıları: ss.63-66
• İstanbul Üniversitesi Adresli: Evet

Özet

Background 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.