Clidocraneal dysostosis: Literature review and report of a clinical case.

Cleidocranial dysostosis (CCD) is a rare congenital skeletal disorder associated to clavicular hypoplasia or aplasia, delayed closure of fontanelles head with brachycephalic type, delayed exfoliation of primary teeth, delayed eruption of permanent teeth, presence of several supernumeraries and morp...

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Main Authors: Bernardita Toro, Antonieta Pérez, Claudia Fierro
Format: Article
Language:English
Published: Universidad de Concepción. 2012-07-01
Series:Journal of Oral Research
Subjects:
Online Access:http://www.joralres.com/index.php/JOR/article/view/6/9
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author Bernardita Toro
Antonieta Pérez
Claudia Fierro
author_facet Bernardita Toro
Antonieta Pérez
Claudia Fierro
author_sort Bernardita Toro
collection DOAJ
description Cleidocranial dysostosis (CCD) is a rare congenital skeletal disorder associated to clavicular hypoplasia or aplasia, delayed closure of fontanelles head with brachycephalic type, delayed exfoliation of primary teeth, delayed eruption of permanent teeth, presence of several supernumeraries and morphological changes on the maxilla and mandible. This disorder is inherited as an autosomal dominant condition and 40% of the cases appear spontaneously without apparent genetic cause. Early diagnosis is very important to give patients the best treatment options. In this article, literature regarding CCD, its etiology, early diagnosis, and general and dental features. A patient with this condition is presented.
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spelling doaj.art-33f2603caee04ec0b4b5d9e1f815958d2022-12-22T01:53:20ZengUniversidad de Concepción.Journal of Oral Research0719-24600719-24792012-07-0111222610.17126/joralres.2012.006Clidocraneal dysostosis: Literature review and report of a clinical case.Bernardita Toro0Antonieta Pérez1Claudia Fierro2Hospital Provincial Dr. Rafael Avaría. Curanilahue, Chile.Facultad de Odontología. Universidad de Concepción, Chile.Facultad de Odontología. Universidad de Concepción, Chile.Cleidocranial dysostosis (CCD) is a rare congenital skeletal disorder associated to clavicular hypoplasia or aplasia, delayed closure of fontanelles head with brachycephalic type, delayed exfoliation of primary teeth, delayed eruption of permanent teeth, presence of several supernumeraries and morphological changes on the maxilla and mandible. This disorder is inherited as an autosomal dominant condition and 40% of the cases appear spontaneously without apparent genetic cause. Early diagnosis is very important to give patients the best treatment options. In this article, literature regarding CCD, its etiology, early diagnosis, and general and dental features. A patient with this condition is presented.http://www.joralres.com/index.php/JOR/article/view/6/9cleidocraneal disostosishypoplasiasupernumerary teeth
spellingShingle Bernardita Toro
Antonieta Pérez
Claudia Fierro
Clidocraneal dysostosis: Literature review and report of a clinical case.
Journal of Oral Research
cleidocraneal disostosis
hypoplasia
supernumerary teeth
title Clidocraneal dysostosis: Literature review and report of a clinical case.
title_full Clidocraneal dysostosis: Literature review and report of a clinical case.
title_fullStr Clidocraneal dysostosis: Literature review and report of a clinical case.
title_full_unstemmed Clidocraneal dysostosis: Literature review and report of a clinical case.
title_short Clidocraneal dysostosis: Literature review and report of a clinical case.
title_sort clidocraneal dysostosis literature review and report of a clinical case
topic cleidocraneal disostosis
hypoplasia
supernumerary teeth
url http://www.joralres.com/index.php/JOR/article/view/6/9
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