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Hereditary Hypotrichosis Simplex of the Scalp

Hereditary hypotrichosis simplex of the scalp is a genetic disorder, characterized by sparse or absent scalp hair without structural defects, in the absence of other ectodermal or systemic abnormalities. Structural hair defects may be presented with a genetic disorder affecting hair growth or part o...

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Autores principales: Moravvej-Farshi, Hamideh, Ayatollahi, Azin, Hejazi, Somayeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248538/
https://www.ncbi.nlm.nih.gov/pubmed/25484430
http://dx.doi.org/10.4103/0019-5154.143586
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author Moravvej-Farshi, Hamideh
Ayatollahi, Azin
Hejazi, Somayeh
author_facet Moravvej-Farshi, Hamideh
Ayatollahi, Azin
Hejazi, Somayeh
author_sort Moravvej-Farshi, Hamideh
collection PubMed
description Hereditary hypotrichosis simplex of the scalp is a genetic disorder, characterized by sparse or absent scalp hair without structural defects, in the absence of other ectodermal or systemic abnormalities. Structural hair defects may be presented with a genetic disorder affecting hair growth or part of a congenital syndrome or may indicate underlying metabolic disorders, or may be associated with other diseases. We describe a 26-years-old Persian girl suffering from hypotrichosis simplex of the scalp with trichorrhexis nodosa who had no ectodermal defects and systemic disease.
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spelling pubmed-42485382014-12-05 Hereditary Hypotrichosis Simplex of the Scalp Moravvej-Farshi, Hamideh Ayatollahi, Azin Hejazi, Somayeh Indian J Dermatol E-IJD Case Report Hereditary hypotrichosis simplex of the scalp is a genetic disorder, characterized by sparse or absent scalp hair without structural defects, in the absence of other ectodermal or systemic abnormalities. Structural hair defects may be presented with a genetic disorder affecting hair growth or part of a congenital syndrome or may indicate underlying metabolic disorders, or may be associated with other diseases. We describe a 26-years-old Persian girl suffering from hypotrichosis simplex of the scalp with trichorrhexis nodosa who had no ectodermal defects and systemic disease. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4248538/ /pubmed/25484430 http://dx.doi.org/10.4103/0019-5154.143586 Text en Copyright: © Indian Journal of Dermatology 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 E-IJD Case Report
Moravvej-Farshi, Hamideh
Ayatollahi, Azin
Hejazi, Somayeh
Hereditary Hypotrichosis Simplex of the Scalp
title Hereditary Hypotrichosis Simplex of the Scalp
title_full Hereditary Hypotrichosis Simplex of the Scalp
title_fullStr Hereditary Hypotrichosis Simplex of the Scalp
title_full_unstemmed Hereditary Hypotrichosis Simplex of the Scalp
title_short Hereditary Hypotrichosis Simplex of the Scalp
title_sort hereditary hypotrichosis simplex of the scalp
topic E-IJD Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248538/
https://www.ncbi.nlm.nih.gov/pubmed/25484430
http://dx.doi.org/10.4103/0019-5154.143586
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