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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...

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Autores principales: Silveira, Laura Maria Andrade, Ramos, Andréia Nogueira, do Amaral, Isadora Rosado, Rêgo, Vitoria Regina Pedreira de Almeida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2013
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.
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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?*
title_full Do you know this syndrome?*
title_fullStr Do you know this syndrome?*
title_full_unstemmed Do you know this syndrome?*
title_short Do you know this syndrome?*
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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