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A 12 year old boy with recurrent episodes of pneumonia: triple A syndrome
Triple A syndrome (Allgrove syndrome) is a rare inherited autosomal recessive disease with a typical triad including adrenocorticotrophic-hormone-resistant glucocorticoid insufficiency, reduced or absent tearing (alacrima) and achalasia and a wide range of symptoms can be detected due to multi organ...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Research Institute for Gastroenterology and Liver Diseases
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017457/ https://www.ncbi.nlm.nih.gov/pubmed/24834210 |
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author | Parhizkar, Baran Maghsoodi, Nakisa Forootan, Mojgan Entezari, Amir Hosein |
author_facet | Parhizkar, Baran Maghsoodi, Nakisa Forootan, Mojgan Entezari, Amir Hosein |
author_sort | Parhizkar, Baran |
collection | PubMed |
description | Triple A syndrome (Allgrove syndrome) is a rare inherited autosomal recessive disease with a typical triad including adrenocorticotrophic-hormone-resistant glucocorticoid insufficiency, reduced or absent tearing (alacrima) and achalasia and a wide range of symptoms can be detected due to multi organ involvement. This report describes the case of a Triple Asyndrome, a12 year-old boy with a history of recurrent episodes of pneumonia and growth retardation due to failure to timely diagnosis of his problem. |
format | Online Article Text |
id | pubmed-4017457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Research Institute for Gastroenterology and Liver Diseases |
record_format | MEDLINE/PubMed |
spelling | pubmed-40174572014-05-15 A 12 year old boy with recurrent episodes of pneumonia: triple A syndrome Parhizkar, Baran Maghsoodi, Nakisa Forootan, Mojgan Entezari, Amir Hosein Gastroenterol Hepatol Bed Bench Case Report Triple A syndrome (Allgrove syndrome) is a rare inherited autosomal recessive disease with a typical triad including adrenocorticotrophic-hormone-resistant glucocorticoid insufficiency, reduced or absent tearing (alacrima) and achalasia and a wide range of symptoms can be detected due to multi organ involvement. This report describes the case of a Triple Asyndrome, a12 year-old boy with a history of recurrent episodes of pneumonia and growth retardation due to failure to timely diagnosis of his problem. Research Institute for Gastroenterology and Liver Diseases 2012 /pmc/articles/PMC4017457/ /pubmed/24834210 Text en Copyright © 2012 Research Institute for Gastroenterology and Liver Diseases http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Case Report Parhizkar, Baran Maghsoodi, Nakisa Forootan, Mojgan Entezari, Amir Hosein A 12 year old boy with recurrent episodes of pneumonia: triple A syndrome |
title | A 12 year old boy with recurrent episodes of pneumonia: triple A syndrome |
title_full | A 12 year old boy with recurrent episodes of pneumonia: triple A syndrome |
title_fullStr | A 12 year old boy with recurrent episodes of pneumonia: triple A syndrome |
title_full_unstemmed | A 12 year old boy with recurrent episodes of pneumonia: triple A syndrome |
title_short | A 12 year old boy with recurrent episodes of pneumonia: triple A syndrome |
title_sort | 12 year old boy with recurrent episodes of pneumonia: triple a syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017457/ https://www.ncbi.nlm.nih.gov/pubmed/24834210 |
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