Application of 3-D Imaging in a Familial Case of Cleidocranial Dysplasia
Abstract
Cleidocranial dysplasia (CCD) is a rare inherited disorder affecting dental and skeletal tissues. CCD usually has an autosomal dominant pattern of inheritance and common clinical features seen are aplastic or hypoplastic clavicles, late closure of fontanelle, open skull sutures, retained deciduous teeth, late eruption of permanent teeth and presence of multiple impacted supernumerary teeth. Here, we present a case of CCD in a female patient with positive family history. The diagnosis was confirmed clinically and radiographically. The newer radiographic advancement, CBCT was used to validate the radiographic findings.
Keywords
Supporting Institution
References
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Details
Primary Language
English
Subjects
Health Care Administration
Journal Section
Case Report
Authors
Renita Castelino
Türkiye
Publication Date
June 30, 2020
Submission Date
December 31, 2019
Acceptance Date
April 2, 2020
Published in Issue
Year 1970 Volume: 23 Number: 2