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


Bayram M., Yildirim M., Seymen F.

EUROPEAN ARCHIVES OF PAEDIATRIC DENTISTRY, cilt.16, ss.63-66, 2015 (ESCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 16 Konu: 1
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1007/s40368-014-0141-0
  • Dergi Adı: EUROPEAN ARCHIVES OF PAEDIATRIC DENTISTRY
  • Sayfa Sayıları: ss.63-66

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.