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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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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. |
format | Online Article Text |
id | pubmed-4248538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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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