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Cleidocranial dysplasia with hearing loss

Cleidocranial dysplasia is an inherited skeletal anomaly that affects primarily the skull, clavicle, and dentition, which can occur spontaneously, but most are inherited in autosomal dominant mode. The skull findings are brachycephaly, delayed or failed closure of the fontanelles, presence of open s...

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Autores principales: Candamourty, Ramesh, Venkatachalam, Suresh, Yuvaraj, Vaithilingam, Kumar, Ganesan Suresh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633291/
https://www.ncbi.nlm.nih.gov/pubmed/23633875
http://dx.doi.org/10.4103/0976-9668.107318
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author Candamourty, Ramesh
Venkatachalam, Suresh
Yuvaraj, Vaithilingam
Kumar, Ganesan Suresh
author_facet Candamourty, Ramesh
Venkatachalam, Suresh
Yuvaraj, Vaithilingam
Kumar, Ganesan Suresh
author_sort Candamourty, Ramesh
collection PubMed
description Cleidocranial dysplasia is an inherited skeletal anomaly that affects primarily the skull, clavicle, and dentition, which can occur spontaneously, but most are inherited in autosomal dominant mode. The skull findings are brachycephaly, delayed or failed closure of the fontanelles, presence of open skull sutures and multiple wormian bones with pronounced frontal bossing. The syndrome is notable for aplasia or hypoplasia of the clavicles. The neck appears long and narrow and the shoulders markedly droop. Oral manifestations exhibit a hypoplastic maxilla with high-arched palate. Crowding of teeth is produced by retention of deciduous teeth, delayed eruption of permanent teeth, and the presence of a large number of unerupted supernumerary teeth. We report a case of CCD in a 12-year-old girl who presented with an unaesthetic facial appearance, unerupted permanent dentition with hearing loss.
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spelling pubmed-36332912013-04-30 Cleidocranial dysplasia with hearing loss Candamourty, Ramesh Venkatachalam, Suresh Yuvaraj, Vaithilingam Kumar, Ganesan Suresh J Nat Sci Biol Med Case Report Cleidocranial dysplasia is an inherited skeletal anomaly that affects primarily the skull, clavicle, and dentition, which can occur spontaneously, but most are inherited in autosomal dominant mode. The skull findings are brachycephaly, delayed or failed closure of the fontanelles, presence of open skull sutures and multiple wormian bones with pronounced frontal bossing. The syndrome is notable for aplasia or hypoplasia of the clavicles. The neck appears long and narrow and the shoulders markedly droop. Oral manifestations exhibit a hypoplastic maxilla with high-arched palate. Crowding of teeth is produced by retention of deciduous teeth, delayed eruption of permanent teeth, and the presence of a large number of unerupted supernumerary teeth. We report a case of CCD in a 12-year-old girl who presented with an unaesthetic facial appearance, unerupted permanent dentition with hearing loss. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3633291/ /pubmed/23633875 http://dx.doi.org/10.4103/0976-9668.107318 Text en Copyright: © Journal of Natural Science, Biology and Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Candamourty, Ramesh
Venkatachalam, Suresh
Yuvaraj, Vaithilingam
Kumar, Ganesan Suresh
Cleidocranial dysplasia with hearing loss
title Cleidocranial dysplasia with hearing loss
title_full Cleidocranial dysplasia with hearing loss
title_fullStr Cleidocranial dysplasia with hearing loss
title_full_unstemmed Cleidocranial dysplasia with hearing loss
title_short Cleidocranial dysplasia with hearing loss
title_sort cleidocranial dysplasia with hearing loss
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633291/
https://www.ncbi.nlm.nih.gov/pubmed/23633875
http://dx.doi.org/10.4103/0976-9668.107318
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