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Do you know this syndrome?()

The hyperimmunoglobulin E syndrome, or Job's syndrome is a rare primary immunodeficiency characterized by recurrent skin abscesses, recurrent respiratory tract infections, and high levels of IgE, eosinophilia, bone and dental changes. We report the case of a fourteen-year-old male patient prese...

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Detalles Bibliográficos
Autores principales: de Lima, Alexandre Moretti, Sperandio, Vitor Arantes, da Rocha, Sheila Pereira, de Ribeiro, Beatriz Medeiros, Reis, Carmelia Matos Santiago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798370/
https://www.ncbi.nlm.nih.gov/pubmed/24173199
http://dx.doi.org/10.1590/abd1806-4841.20132112
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author de Lima, Alexandre Moretti
Sperandio, Vitor Arantes
da Rocha, Sheila Pereira
de Ribeiro, Beatriz Medeiros
Reis, Carmelia Matos Santiago
author_facet de Lima, Alexandre Moretti
Sperandio, Vitor Arantes
da Rocha, Sheila Pereira
de Ribeiro, Beatriz Medeiros
Reis, Carmelia Matos Santiago
author_sort de Lima, Alexandre Moretti
collection PubMed
description The hyperimmunoglobulin E syndrome, or Job's syndrome is a rare primary immunodeficiency characterized by recurrent skin abscesses, recurrent respiratory tract infections, and high levels of IgE, eosinophilia, bone and dental changes. We report the case of a fourteen-year-old male patient presenting this disease, with both typical and also some relatively sporadic manifestations. We performed a literature review on the syndrome and its associated clinical findings.
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spelling pubmed-37983702013-10-25 Do you know this syndrome?() de Lima, Alexandre Moretti Sperandio, Vitor Arantes da Rocha, Sheila Pereira de Ribeiro, Beatriz Medeiros Reis, Carmelia Matos Santiago An Bras Dermatol Syndrome in Question The hyperimmunoglobulin E syndrome, or Job's syndrome is a rare primary immunodeficiency characterized by recurrent skin abscesses, recurrent respiratory tract infections, and high levels of IgE, eosinophilia, bone and dental changes. We report the case of a fourteen-year-old male patient presenting this disease, with both typical and also some relatively sporadic manifestations. We performed a literature review on the syndrome and its associated clinical findings. Sociedade Brasileira de Dermatologia 2013 /pmc/articles/PMC3798370/ /pubmed/24173199 http://dx.doi.org/10.1590/abd1806-4841.20132112 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
de Lima, Alexandre Moretti
Sperandio, Vitor Arantes
da Rocha, Sheila Pereira
de Ribeiro, Beatriz Medeiros
Reis, Carmelia Matos Santiago
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/PMC3798370/
https://www.ncbi.nlm.nih.gov/pubmed/24173199
http://dx.doi.org/10.1590/abd1806-4841.20132112
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