Ectodermal dysplasia - A rare case report

Ectodermal dysplasia (ED) is a rare genetic disease caused by developmental disturbances of embryonic ectoderm derived tissues, organs, and other accessory appendages. The congenital missing of teeth is usually bilateral. Anodontia or hypodontia may be associated with other ectodermal disturbances,...

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Autores principales: Bhakta, Poulomi, Barthunia, Bhavna, Nigam, Haritma, Pawar, Pallavi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820434/
https://www.ncbi.nlm.nih.gov/pubmed/31681695
http://dx.doi.org/10.4103/jfmpc.jfmpc_625_19
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author Bhakta, Poulomi
Barthunia, Bhavna
Nigam, Haritma
Pawar, Pallavi
author_facet Bhakta, Poulomi
Barthunia, Bhavna
Nigam, Haritma
Pawar, Pallavi
author_sort Bhakta, Poulomi
collection PubMed
description Ectodermal dysplasia (ED) is a rare genetic disease caused by developmental disturbances of embryonic ectoderm derived tissues, organs, and other accessory appendages. The congenital missing of teeth is usually bilateral. Anodontia or hypodontia may be associated with other ectodermal disturbances, such as anhidrosis, asteatosis, hypotrichosis, and salivary glands defects. One such case report of ED is demonstrated here.
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spelling pubmed-68204342019-11-01 Ectodermal dysplasia - A rare case report Bhakta, Poulomi Barthunia, Bhavna Nigam, Haritma Pawar, Pallavi J Family Med Prim Care Case Report Ectodermal dysplasia (ED) is a rare genetic disease caused by developmental disturbances of embryonic ectoderm derived tissues, organs, and other accessory appendages. The congenital missing of teeth is usually bilateral. Anodontia or hypodontia may be associated with other ectodermal disturbances, such as anhidrosis, asteatosis, hypotrichosis, and salivary glands defects. One such case report of ED is demonstrated here. Wolters Kluwer - Medknow 2019-09-30 /pmc/articles/PMC6820434/ /pubmed/31681695 http://dx.doi.org/10.4103/jfmpc.jfmpc_625_19 Text en Copyright: © 2019 Journal of Family Medicine and Primary Care http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Bhakta, Poulomi
Barthunia, Bhavna
Nigam, Haritma
Pawar, Pallavi
Ectodermal dysplasia - A rare case report
title Ectodermal dysplasia - A rare case report
title_full Ectodermal dysplasia - A rare case report
title_fullStr Ectodermal dysplasia - A rare case report
title_full_unstemmed Ectodermal dysplasia - A rare case report
title_short Ectodermal dysplasia - A rare case report
title_sort ectodermal dysplasia - a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820434/
https://www.ncbi.nlm.nih.gov/pubmed/31681695
http://dx.doi.org/10.4103/jfmpc.jfmpc_625_19
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AT barthuniabhavna ectodermaldysplasiaararecasereport
AT nigamharitma ectodermaldysplasiaararecasereport
AT pawarpallavi ectodermaldysplasiaararecasereport

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