1990 Volume 36 Issue 6 Pages 1483-1488
We experienced two cases of cleidocranial dysostosis, which is characterized by defect of clavicle, skull deformities, dental abnormalities and hereditary. However, several cases had no hereditary in the past reports. Likewise, in our cases, one patient had a family history that was suspected of hereditary but the other patient had no particular family history.
When family history is suspected, we have to examine the family, especially young family of the patient, because we then can select the appropriate therapy for dental abnormalities by early diagnosis. In this report, we discuss the therapy for dental abnormalities in view of early diagnosis.