Displasia cleidocraneal: presentación de un caso

Cleidocranial dysplasia is a skeletal dysplasia characterized by autosomal dominant inheritance, cranial abnormalities, clavicular, and dental, caused by mutations or deletions in RUNX2 gene. We report the case of a girl of 6.5 years attended our submitted by delayed closure of the anterior fontanelle and ossification of the pelvis, in whom diagnosis is done by clinical and radiological findings.