The KBG syndrome, characteristic dental findings: a case report

Int J Paediatr Dent. 2001 Mar;11(2):131-4. doi: 10.1046/j.1365-263x.2001.00231.x.

Abstract

Short stature and developmental delay may be observed in many genetic conditions and well-defined syndromes. A 7-year-old girl presented with the non-specific findings of subtle dysmorphism, short stature and developmental delay. Although a genetic syndrome was suspected, a definitive diagnosis was not made until the dental findings of KBG syndrome were recognised, namely grossly enlarged maxillary permanent central incisors and hypodontia.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple*
  • Child
  • Dental Pulp Cavity / abnormalities
  • Developmental Disabilities
  • Dwarfism
  • Facies
  • Female
  • Humans
  • Incisor / abnormalities
  • Syndrome
  • Tooth Abnormalities* / pathology