Kosar, ShaminaShah, AjazFarooq, ShahidGul, SumeraBashir, Shabroza2019-12-062019-12-062018-11Kosar Shamina, Shah Ajaz, Farooq Shahid, Gul Sumera, Bashir Shabroza. Cleidocranial Dysplasia - A Rare Case Report. Annals of International medical and Dental Research. 2018 Nov; 4(11): 5-72395-28222395-2814http://imsear.searo.who.int/handle/123456789/188402Cleidocranial dysplasia is an autosomal dominant heritable disorder caused by mutation in the gene encoding transcription factor Core Binding Factor Subunit Alpha 1 (CBFA1) or Runt related transcription factor 2 (RUNX2). It is characterized by aplasia or hypoplasia of the clavicles, characteristic craniofacial malformations, and the presence of numerous supernumerary and unerupted teeth. A 37 year old male with cleidocranial dysplasia is described in this article with cyst associated with impacted teeth as the first presentation.Journal ArticleIndiaPost Graduate, Department of Oral and Maxillofacial Surgery, Government Dental College, Srinagar