Translated title of the contribution: Odontochondrodysplasia

P. Maroteaux, V. Briscioli, F. Lalatta, J. Bonaventure

Research output: Contribution to journalArticlepeer-review


Background. - Dentinogenesis imperfecta is exceptionally associated to chondrodysplasia. The aim of this work is to present four cases of such an association. Cases report. - These four children (three boys; one girl) suffered from growth retardation, ligamentous hyperlaxity, scoliosis. Main features were present since the first months of life. Dentinogenesis imperfecta was more marked on the first teeth, On X-rays, all patients had short tubular bones, more pronounced at the level of the middle segment of their limbs, with irregular metaphyses. Cone-shaped epiphyses were present on the hands. Iliac wings were square-shaped and vertebral bodies had a posterior wedging. Conclusion. - These four cases, including two previously published as Goldblatt's syndrome, share the same findings as another case described by this author. We propose the name of odontochondrodysplasia for this apparently unfortuitous association: dentinogenesis imperfecta and chondrodysplasia.

Translated title of the contributionOdontochondrodysplasia
Original languageFrench
Pages (from-to)549-554
Number of pages6
JournalArchives de Pediatrie
Issue number6
Publication statusPublished - Jun 1996


  • bone disease, developmental
  • child
  • chondrodysplasia
  • dentinogenesis
  • dwarfism
  • ligaments
  • odontochondrodyspla sia
  • scoliosis

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health


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