Disostose cleidocraniana: relato de dois casos familiares

Cleidocranial dysostosis is a rare genetic syndrome with an autosomal dominant inheritance pattern. The most common manifestations include clavicular aplasia or hypoplasia, open fontanelles and abnormal dentition. The present report describes two familial cases whose late diagnosis was made by means of clinical and radiographic findings. The treatment was radical, with complete surgical teeth extraction and making of total dental prosthesis.

• Assuntos:

  • Disostose cleidocraniana
  • Hipoplasia de clavícula
  • Dentes extranumerários