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Ectodermal dysplasia – Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature

Ectodermal dysplasia is a rare group of inherited disorders characterized by aplasia or dysplasia of tissues of ectodermal origin, such as hair, nails, teeth and skin. Dental manifestations include hypodontia, complete anodontia or malformed teeth. Oral rehabilitation is the major surgical challenge...

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Detalles Bibliográficos
Autores principales: Deshpande, Sanjeev N., Kumar, Vikas
Formato: Texto
Lenguaje:English
Publicado: Medknow Publication 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2938635/
https://www.ncbi.nlm.nih.gov/pubmed/20924460
http://dx.doi.org/10.4103/0970-0358.63969
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author Deshpande, Sanjeev N.
Kumar, Vikas
author_facet Deshpande, Sanjeev N.
Kumar, Vikas
author_sort Deshpande, Sanjeev N.
collection PubMed
description Ectodermal dysplasia is a rare group of inherited disorders characterized by aplasia or dysplasia of tissues of ectodermal origin, such as hair, nails, teeth and skin. Dental manifestations include hypodontia, complete anodontia or malformed teeth. Oral rehabilitation is the major surgical challenge in such patients. It frequently requires alveolar reconstruction followed by dental implants. We report a case of hypohidrotic ectodermal dysplasia, which was managed with reconstruction of both the upper and the lower alveolus using free fibula flaps with dental rehabilitation using osseointegrated implants.
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spelling pubmed-29386352010-10-05 Ectodermal dysplasia – Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature Deshpande, Sanjeev N. Kumar, Vikas Indian J Plast Surg Case Report Ectodermal dysplasia is a rare group of inherited disorders characterized by aplasia or dysplasia of tissues of ectodermal origin, such as hair, nails, teeth and skin. Dental manifestations include hypodontia, complete anodontia or malformed teeth. Oral rehabilitation is the major surgical challenge in such patients. It frequently requires alveolar reconstruction followed by dental implants. We report a case of hypohidrotic ectodermal dysplasia, which was managed with reconstruction of both the upper and the lower alveolus using free fibula flaps with dental rehabilitation using osseointegrated implants. Medknow Publication 2010 /pmc/articles/PMC2938635/ /pubmed/20924460 http://dx.doi.org/10.4103/0970-0358.63969 Text en © Indian Journal of Plastic Surgery http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of 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
Deshpande, Sanjeev N.
Kumar, Vikas
Ectodermal dysplasia – Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature
title Ectodermal dysplasia – Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature
title_full Ectodermal dysplasia – Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature
title_fullStr Ectodermal dysplasia – Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature
title_full_unstemmed Ectodermal dysplasia – Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature
title_short Ectodermal dysplasia – Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature
title_sort ectodermal dysplasia – maxillary and mandibular alveolar reconstruction with dental rehabilitation: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2938635/
https://www.ncbi.nlm.nih.gov/pubmed/20924460
http://dx.doi.org/10.4103/0970-0358.63969
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