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Mundlos, S., Mulliken, J.B., Abramson, D.L., Warman, M.L., Knoll, J.H., and Olsen, B.R. Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion Dental abnormalities in cleidocranial dysplasia in one family. Hum Mol Genet. 1995; 4: 71-75.

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Article

A 9-year-old Saudi Boy with Cleidocranial Dysplasia: A Case Report

1Saudi Pediatric Dentistry Program, Dammam Medical Complex, Dammam, Kingdom of Saudi Arabia (KSA)

2Department of dentistry, King Fahd Military Medical Complex, Dhahran, KSA

3Department of Dentistry, University of Hail, KSA

4College of Medicine, University of Hail, KSA


American Journal of Medical Case Reports. 2017, Vol. 5 No. 11, 270-273
DOI: 10.12691/ajmcr-5-11-1
Copyright © 2017 Science and Education Publishing

Cite this paper:
Rabab Ali Jassim AL Buainain, Yasin Alavi Aruveetil, Faisal Alsineedi, Abdullah Faraj Alshammari, Hussain Gadelkarim Ahmed. A 9-year-old Saudi Boy with Cleidocranial Dysplasia: A Case Report. American Journal of Medical Case Reports. 2017; 5(11):270-273. doi: 10.12691/ajmcr-5-11-1.

Correspondence to: Hussain  Gadelkarim Ahmed, College of Medicine, University of Hail, KSA. Email: hussaingad1972@yahoo.com

Abstract

Cleidocranial dysplasia (CCD) is an uncommon disorder associated with a genetic disorder mainly causing dysplasia of bones and teeth with autosomal dominant inheritance pattern, which has an extremely varied presentation. The dental indicators are principally delayed exfoliation of primary teeth and delayed eruption of permanent teeth, and numerous impacted supernumeraries. This article represent a 9 years old Saudi boy case of CCD and illustrates the clinical and radiological features of this patients. In this case the early diagnosis of the condition was not associated with proper orientation of the dental treatment to offer better quality of life to patient.

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