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Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness()()
Monilethrix is a rare defect of the hair shaft, with most cases showing an autosomal dominant pattern of inheritance and variable clinical expression. It is characterized by hypotrichosis secondary to hair fragility. The diagnosis is made through trichoscopy, detecting typical findings such as perio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441526/ https://www.ncbi.nlm.nih.gov/pubmed/34272078 http://dx.doi.org/10.1016/j.abd.2020.07.019 |
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author | Antoniali, Daniela Westin, Andrezza Telles Cruz, Fernanda André Martins Simão, João Carlos Lopes |
author_facet | Antoniali, Daniela Westin, Andrezza Telles Cruz, Fernanda André Martins Simão, João Carlos Lopes |
author_sort | Antoniali, Daniela |
collection | PubMed |
description | Monilethrix is a rare defect of the hair shaft, with most cases showing an autosomal dominant pattern of inheritance and variable clinical expression. It is characterized by hypotrichosis secondary to hair fragility. The diagnosis is made through trichoscopy, detecting typical findings such as periodic narrowing at regular intervals, giving the hair the appearance of beads in a rosary. This article reports the case of six members of a family diagnosed with monilethrix with alopecia of varying degrees. |
format | Online Article Text |
id | pubmed-8441526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-84415262021-09-20 Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness()() Antoniali, Daniela Westin, Andrezza Telles Cruz, Fernanda André Martins Simão, João Carlos Lopes An Bras Dermatol Case Report Monilethrix is a rare defect of the hair shaft, with most cases showing an autosomal dominant pattern of inheritance and variable clinical expression. It is characterized by hypotrichosis secondary to hair fragility. The diagnosis is made through trichoscopy, detecting typical findings such as periodic narrowing at regular intervals, giving the hair the appearance of beads in a rosary. This article reports the case of six members of a family diagnosed with monilethrix with alopecia of varying degrees. Sociedade Brasileira de Dermatologia 2021 2021-07-14 /pmc/articles/PMC8441526/ /pubmed/34272078 http://dx.doi.org/10.1016/j.abd.2020.07.019 Text en © 2021 Sociedade Brasileira de Dermatologia. Published by Elsevier España, S.L.U. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Antoniali, Daniela Westin, Andrezza Telles Cruz, Fernanda André Martins Simão, João Carlos Lopes Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness()() |
title | Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness()() |
title_full | Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness()() |
title_fullStr | Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness()() |
title_full_unstemmed | Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness()() |
title_short | Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness()() |
title_sort | moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness()() |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441526/ https://www.ncbi.nlm.nih.gov/pubmed/34272078 http://dx.doi.org/10.1016/j.abd.2020.07.019 |
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