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Hair Shaft Disorders in Children – An Update

Disorders of hair shaft are a diverse group of congenital and acquired abnormalities of the hair that can pose a diagnostic and therapeutic challenge to the dermatologists. Hair shaft abnormalities can occur as an isolated phenomenon or can be associated with an underlying genetic syndrome. Any chan...

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Autores principales: Bhat, Yasmeen Jabeen, Trumboo, Taiba, Krishan, Kewal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115339/
https://www.ncbi.nlm.nih.gov/pubmed/37089857
http://dx.doi.org/10.4103/idoj.idoj_7_22
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author Bhat, Yasmeen Jabeen
Trumboo, Taiba
Krishan, Kewal
author_facet Bhat, Yasmeen Jabeen
Trumboo, Taiba
Krishan, Kewal
author_sort Bhat, Yasmeen Jabeen
collection PubMed
description Disorders of hair shaft are a diverse group of congenital and acquired abnormalities of the hair that can pose a diagnostic and therapeutic challenge to the dermatologists. Hair shaft abnormalities can occur as an isolated phenomenon or can be associated with an underlying genetic syndrome. Any change in the texture, appearance, and growth of the hair should prompt evaluation of the patient for the presence of any hair shaft anomaly. The diagnosis can be suggested by a complete history and physical examination of the hair-bearing areas as well as other ectodermal structures (nails and teeth). A key feature in the evaluation of hair shaft defects is to determine the fragility of the hair shaft that can be elucidated by performing the “tug test.” Trichoscopy and light microscopy serve as valuable tools in establishing the specific type of hair shaft disorder. An update of the approach for the diagnosis and management is included in this review.
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spelling pubmed-101153392023-04-20 Hair Shaft Disorders in Children – An Update Bhat, Yasmeen Jabeen Trumboo, Taiba Krishan, Kewal Indian Dermatol Online J Review Article Disorders of hair shaft are a diverse group of congenital and acquired abnormalities of the hair that can pose a diagnostic and therapeutic challenge to the dermatologists. Hair shaft abnormalities can occur as an isolated phenomenon or can be associated with an underlying genetic syndrome. Any change in the texture, appearance, and growth of the hair should prompt evaluation of the patient for the presence of any hair shaft anomaly. The diagnosis can be suggested by a complete history and physical examination of the hair-bearing areas as well as other ectodermal structures (nails and teeth). A key feature in the evaluation of hair shaft defects is to determine the fragility of the hair shaft that can be elucidated by performing the “tug test.” Trichoscopy and light microscopy serve as valuable tools in establishing the specific type of hair shaft disorder. An update of the approach for the diagnosis and management is included in this review. Wolters Kluwer - Medknow 2023-02-23 /pmc/articles/PMC10115339/ /pubmed/37089857 http://dx.doi.org/10.4103/idoj.idoj_7_22 Text en Copyright: © 2023 Indian Dermatology Online Journal https://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 Review Article
Bhat, Yasmeen Jabeen
Trumboo, Taiba
Krishan, Kewal
Hair Shaft Disorders in Children – An Update
title Hair Shaft Disorders in Children – An Update
title_full Hair Shaft Disorders in Children – An Update
title_fullStr Hair Shaft Disorders in Children – An Update
title_full_unstemmed Hair Shaft Disorders in Children – An Update
title_short Hair Shaft Disorders in Children – An Update
title_sort hair shaft disorders in children – an update
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115339/
https://www.ncbi.nlm.nih.gov/pubmed/37089857
http://dx.doi.org/10.4103/idoj.idoj_7_22
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