Ectodermal dysplasia (ED) syndrome

Ectodermal dysplasia (ED) syndrome comprises a large, heterogeneous group of inherited disorders that are defined by primary defects in the development of 2 or more tissues derived from the embryonic ectoderm. The tissues primarily involved are the skin and its appendages (including hair follicles,...

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Detalles Bibliográficos
Autores principales: Chee, Siew-Yin, Wanga, Chung-Hsing, Lina, Wei-De, Tsaia, Fuu-Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: China Medical University 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264978/
https://www.ncbi.nlm.nih.gov/pubmed/25520940
http://dx.doi.org/10.7603/s40681-014-0027-9
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author Chee, Siew-Yin
Wanga, Chung-Hsing
Lina, Wei-De
Tsaia, Fuu-Jen
author_facet Chee, Siew-Yin
Wanga, Chung-Hsing
Lina, Wei-De
Tsaia, Fuu-Jen
author_sort Chee, Siew-Yin
collection PubMed
description Ectodermal dysplasia (ED) syndrome comprises a large, heterogeneous group of inherited disorders that are defined by primary defects in the development of 2 or more tissues derived from the embryonic ectoderm. The tissues primarily involved are the skin and its appendages (including hair follicles, eccrine glands, sebaceous glands, nails) and teeth. The clinical features include sparse hair, abnormal or missing teeth, and an inability to sweat due to lack of sweat glands. One such case report of ectodermal dysplasia is presented here.
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spelling pubmed-42649782014-12-15 Ectodermal dysplasia (ED) syndrome Chee, Siew-Yin Wanga, Chung-Hsing Lina, Wei-De Tsaia, Fuu-Jen Biomedicine (Taipei) Original Article Ectodermal dysplasia (ED) syndrome comprises a large, heterogeneous group of inherited disorders that are defined by primary defects in the development of 2 or more tissues derived from the embryonic ectoderm. The tissues primarily involved are the skin and its appendages (including hair follicles, eccrine glands, sebaceous glands, nails) and teeth. The clinical features include sparse hair, abnormal or missing teeth, and an inability to sweat due to lack of sweat glands. One such case report of ectodermal dysplasia is presented here. China Medical University 2014-11-26 /pmc/articles/PMC4264978/ /pubmed/25520940 http://dx.doi.org/10.7603/s40681-014-0027-9 Text en © China Medical University 2014 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided original author(s) and source are credited.
spellingShingle Original Article
Chee, Siew-Yin
Wanga, Chung-Hsing
Lina, Wei-De
Tsaia, Fuu-Jen
Ectodermal dysplasia (ED) syndrome
title Ectodermal dysplasia (ED) syndrome
title_full Ectodermal dysplasia (ED) syndrome
title_fullStr Ectodermal dysplasia (ED) syndrome
title_full_unstemmed Ectodermal dysplasia (ED) syndrome
title_short Ectodermal dysplasia (ED) syndrome
title_sort ectodermal dysplasia (ed) syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264978/
https://www.ncbi.nlm.nih.gov/pubmed/25520940
http://dx.doi.org/10.7603/s40681-014-0027-9
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AT wangachunghsing ectodermaldysplasiaedsyndrome
AT linaweide ectodermaldysplasiaedsyndrome
AT tsaiafuujen ectodermaldysplasiaedsyndrome

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