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Hypohidrotic Ectodermal Dysplasia

Ectodermal dysplasias (ED) are a group of inherited disorders characterized by dysplasia of structures of ectodermal origin, clinically classified into hypohidrotic and hidrotic forms. A 21-year-old female presented with history of hypohidrosis, thinning of scalp and eyebrow hair, xerotic skin, and...

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Autores principales: Bansal, Manish, Manchanda, Kajal, Pandey, Shyam Sunder
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500057/
https://www.ncbi.nlm.nih.gov/pubmed/23180927
http://dx.doi.org/10.4103/0974-7753.100084
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author Bansal, Manish
Manchanda, Kajal
Pandey, Shyam Sunder
author_facet Bansal, Manish
Manchanda, Kajal
Pandey, Shyam Sunder
author_sort Bansal, Manish
collection PubMed
description Ectodermal dysplasias (ED) are a group of inherited disorders characterized by dysplasia of structures of ectodermal origin, clinically classified into hypohidrotic and hidrotic forms. A 21-year-old female presented with history of hypohidrosis, thinning of scalp and eyebrow hair, xerotic skin, and periorbital and perioral wrinkling. There was hypodontia and peg-shaped teeth on intraoral examination. Routine investigations were normal, orthopantomogram revealed absence of multiple teeth with peg-shaped teeth. Histopathological examination showed thinned epidermis and reduction in the number of eccrine units. Thus, the diagnosis was confirmed as Hypohidrotic ED.
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spelling pubmed-35000572012-11-23 Hypohidrotic Ectodermal Dysplasia Bansal, Manish Manchanda, Kajal Pandey, Shyam Sunder Int J Trichology Case Report Ectodermal dysplasias (ED) are a group of inherited disorders characterized by dysplasia of structures of ectodermal origin, clinically classified into hypohidrotic and hidrotic forms. A 21-year-old female presented with history of hypohidrosis, thinning of scalp and eyebrow hair, xerotic skin, and periorbital and perioral wrinkling. There was hypodontia and peg-shaped teeth on intraoral examination. Routine investigations were normal, orthopantomogram revealed absence of multiple teeth with peg-shaped teeth. Histopathological examination showed thinned epidermis and reduction in the number of eccrine units. Thus, the diagnosis was confirmed as Hypohidrotic ED. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3500057/ /pubmed/23180927 http://dx.doi.org/10.4103/0974-7753.100084 Text en Copyright: © International Journal of Trichology 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
Bansal, Manish
Manchanda, Kajal
Pandey, Shyam Sunder
Hypohidrotic Ectodermal Dysplasia
title Hypohidrotic Ectodermal Dysplasia
title_full Hypohidrotic Ectodermal Dysplasia
title_fullStr Hypohidrotic Ectodermal Dysplasia
title_full_unstemmed Hypohidrotic Ectodermal Dysplasia
title_short Hypohidrotic Ectodermal Dysplasia
title_sort hypohidrotic ectodermal dysplasia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500057/
https://www.ncbi.nlm.nih.gov/pubmed/23180927
http://dx.doi.org/10.4103/0974-7753.100084
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