The KBG syndrome: an additional sporadic case

Genet Couns. 2000;11(1):33-5.

Abstract

We report the sporadic case of a boy with clinical features of KBG syndrome, including slight mental retardation, characteristic facies, macrodontia, and skeletal anomalies.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Bone and Bones / abnormalities*
  • Child
  • Hand Deformities, Congenital / genetics*
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Syndrome
  • Tooth Abnormalities / genetics*