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Mild Form of Treacher Collins Syndrome Imitating Juvenile Otosclerosis

Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals with TCS have conductive hearing loss attributed to external and middle ear anomalies. Mild cases of TCS often pass undiagnosed at birth or early childhood. The disease may be manifested as conductiv...

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Detalles Bibliográficos
Autores principales: Zeleník, Karol, Komínek, Pavel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431054/
https://www.ncbi.nlm.nih.gov/pubmed/22953143
http://dx.doi.org/10.1155/2012/616797
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author Zeleník, Karol
Komínek, Pavel
author_facet Zeleník, Karol
Komínek, Pavel
author_sort Zeleník, Karol
collection PubMed
description Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals with TCS have conductive hearing loss attributed to external and middle ear anomalies. Mild cases of TCS often pass undiagnosed at birth or early childhood. The disease may be manifested as conductive hearing loss in teenagers and may resemble juvenile otosclerosis. Patients could suffer from slight facial variabilities including retrognathia (as in our case) and others, which point out to a possible middle ear anomaly. Surgical corrections of middle ear anomalies including TCS generally lead to poorer outcomes comparing with juvenile otosclerosis, which should be discussed with parents during preoperative counselling.
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spelling pubmed-34310542012-09-05 Mild Form of Treacher Collins Syndrome Imitating Juvenile Otosclerosis Zeleník, Karol Komínek, Pavel Case Rep Pediatr Case Report Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals with TCS have conductive hearing loss attributed to external and middle ear anomalies. Mild cases of TCS often pass undiagnosed at birth or early childhood. The disease may be manifested as conductive hearing loss in teenagers and may resemble juvenile otosclerosis. Patients could suffer from slight facial variabilities including retrognathia (as in our case) and others, which point out to a possible middle ear anomaly. Surgical corrections of middle ear anomalies including TCS generally lead to poorer outcomes comparing with juvenile otosclerosis, which should be discussed with parents during preoperative counselling. Hindawi Publishing Corporation 2012 2012-08-16 /pmc/articles/PMC3431054/ /pubmed/22953143 http://dx.doi.org/10.1155/2012/616797 Text en Copyright © 2012 K. Zeleník and P. Komínek. 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
Zeleník, Karol
Komínek, Pavel
Mild Form of Treacher Collins Syndrome Imitating Juvenile Otosclerosis
title Mild Form of Treacher Collins Syndrome Imitating Juvenile Otosclerosis
title_full Mild Form of Treacher Collins Syndrome Imitating Juvenile Otosclerosis
title_fullStr Mild Form of Treacher Collins Syndrome Imitating Juvenile Otosclerosis
title_full_unstemmed Mild Form of Treacher Collins Syndrome Imitating Juvenile Otosclerosis
title_short Mild Form of Treacher Collins Syndrome Imitating Juvenile Otosclerosis
title_sort mild form of treacher collins syndrome imitating juvenile otosclerosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431054/
https://www.ncbi.nlm.nih.gov/pubmed/22953143
http://dx.doi.org/10.1155/2012/616797
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