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Do you know this syndrome?*
Congenital Hypertrichosis Lanugionsa is a rare autosomal dominant genetic disorder, with fewer than 50 cases reported in the literature. It is characterized by excessive lanugo hair, sparing only the mucous membranes, palms and soles. It may be associated with other organic abnormalities and should...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Sociedade Brasileira de Dermatologia
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3754390/ https://www.ncbi.nlm.nih.gov/pubmed/23793217 http://dx.doi.org/10.1590/abd1806-4841.20131965 |
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author | Silveira, Laura Maria Andrade Ramos, Andréia Nogueira do Amaral, Isadora Rosado Rêgo, Vitoria Regina Pedreira de Almeida |
author_facet | Silveira, Laura Maria Andrade Ramos, Andréia Nogueira do Amaral, Isadora Rosado Rêgo, Vitoria Regina Pedreira de Almeida |
author_sort | Silveira, Laura Maria Andrade |
collection | PubMed |
description | Congenital Hypertrichosis Lanugionsa is a rare autosomal dominant genetic disorder, with fewer than 50 cases reported in the literature. It is characterized by excessive lanugo hair, sparing only the mucous membranes, palms and soles. It may be associated with other organic abnormalities and should form part of the dermatologist's current knowledge. We discuss some aspects of the syndrome in question arising from the case report of a 2-year-old female patient, black, with classic clinical presentation, with no other associated congenital abnormalities. |
format | Online Article Text |
id | pubmed-3754390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-37543902013-09-16 Do you know this syndrome?* Silveira, Laura Maria Andrade Ramos, Andréia Nogueira do Amaral, Isadora Rosado Rêgo, Vitoria Regina Pedreira de Almeida An Bras Dermatol Syndrome In Question Congenital Hypertrichosis Lanugionsa is a rare autosomal dominant genetic disorder, with fewer than 50 cases reported in the literature. It is characterized by excessive lanugo hair, sparing only the mucous membranes, palms and soles. It may be associated with other organic abnormalities and should form part of the dermatologist's current knowledge. We discuss some aspects of the syndrome in question arising from the case report of a 2-year-old female patient, black, with classic clinical presentation, with no other associated congenital abnormalities. Sociedade Brasileira de Dermatologia 2013 /pmc/articles/PMC3754390/ /pubmed/23793217 http://dx.doi.org/10.1590/abd1806-4841.20131965 Text en ©2013 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Syndrome In Question Silveira, Laura Maria Andrade Ramos, Andréia Nogueira do Amaral, Isadora Rosado Rêgo, Vitoria Regina Pedreira de Almeida Do you know this syndrome?* |
title | Do you know this syndrome?*
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title_full | Do you know this syndrome?*
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title_fullStr | Do you know this syndrome?*
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title_full_unstemmed | Do you know this syndrome?*
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title_short | Do you know this syndrome?*
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title_sort | do you know this syndrome?* |
topic | Syndrome In Question |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3754390/ https://www.ncbi.nlm.nih.gov/pubmed/23793217 http://dx.doi.org/10.1590/abd1806-4841.20131965 |
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