Hypodontia and Delayed Dentition as the Primary Manifestation of Cleidocranial Dysplasia Presenting with a Diagnostic Dilemma

Cleidocranial dysplasia is a rare autosomal disorder which manifests as partial or complete absence of clavicles, multiple supernumerary teeth, and delayed closure of fontanelle. Classical cases of cleidocranial dysplasia are easily diagnosed very early in the life. However, cases with partial manif...

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Autores principales: Chopra, Radhika, Marwaha, Mohita, Chaudhuri, Payal, Bansal, Kalpana, Chopra, Saurabh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540686/
https://www.ncbi.nlm.nih.gov/pubmed/23320199
http://dx.doi.org/10.1155/2012/262043
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author Chopra, Radhika
Marwaha, Mohita
Chaudhuri, Payal
Bansal, Kalpana
Chopra, Saurabh
author_facet Chopra, Radhika
Marwaha, Mohita
Chaudhuri, Payal
Bansal, Kalpana
Chopra, Saurabh
author_sort Chopra, Radhika
collection PubMed
description Cleidocranial dysplasia is a rare autosomal disorder which manifests as partial or complete absence of clavicles, multiple supernumerary teeth, and delayed closure of fontanelle. Classical cases of cleidocranial dysplasia are easily diagnosed very early in the life. However, cases with partial manifestation of the syndrome and noncontributory family history are difficult to diagnose. Here, we report a case of 8.5-year-old girl child who presented with delayed tooth development (without any supernumerary teeth), anterior open fontanelle, and normal clavicles, thus resulting in a diagnostic dilemma.
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spelling pubmed-35406862013-01-14 Hypodontia and Delayed Dentition as the Primary Manifestation of Cleidocranial Dysplasia Presenting with a Diagnostic Dilemma Chopra, Radhika Marwaha, Mohita Chaudhuri, Payal Bansal, Kalpana Chopra, Saurabh Case Rep Dent Case Report Cleidocranial dysplasia is a rare autosomal disorder which manifests as partial or complete absence of clavicles, multiple supernumerary teeth, and delayed closure of fontanelle. Classical cases of cleidocranial dysplasia are easily diagnosed very early in the life. However, cases with partial manifestation of the syndrome and noncontributory family history are difficult to diagnose. Here, we report a case of 8.5-year-old girl child who presented with delayed tooth development (without any supernumerary teeth), anterior open fontanelle, and normal clavicles, thus resulting in a diagnostic dilemma. Hindawi Publishing Corporation 2012 2012-12-25 /pmc/articles/PMC3540686/ /pubmed/23320199 http://dx.doi.org/10.1155/2012/262043 Text en Copyright © 2012 Radhika Chopra et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Chopra, Radhika
Marwaha, Mohita
Chaudhuri, Payal
Bansal, Kalpana
Chopra, Saurabh
Hypodontia and Delayed Dentition as the Primary Manifestation of Cleidocranial Dysplasia Presenting with a Diagnostic Dilemma
title Hypodontia and Delayed Dentition as the Primary Manifestation of Cleidocranial Dysplasia Presenting with a Diagnostic Dilemma
title_full Hypodontia and Delayed Dentition as the Primary Manifestation of Cleidocranial Dysplasia Presenting with a Diagnostic Dilemma
title_fullStr Hypodontia and Delayed Dentition as the Primary Manifestation of Cleidocranial Dysplasia Presenting with a Diagnostic Dilemma
title_full_unstemmed Hypodontia and Delayed Dentition as the Primary Manifestation of Cleidocranial Dysplasia Presenting with a Diagnostic Dilemma
title_short Hypodontia and Delayed Dentition as the Primary Manifestation of Cleidocranial Dysplasia Presenting with a Diagnostic Dilemma
title_sort hypodontia and delayed dentition as the primary manifestation of cleidocranial dysplasia presenting with a diagnostic dilemma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540686/
https://www.ncbi.nlm.nih.gov/pubmed/23320199
http://dx.doi.org/10.1155/2012/262043
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