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Kawasaki disease in a girl with turner syndrome: a remarkable association
We describe a girl with Turner syndrome, a genetic disorder of the X chromosome in a phenotypic female at increased risk of autoimmune and immunological diseases, who developed Kawasaki disease at the age of four years. Given the possible relationship between these two disorders, we recommend suspec...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944673/ https://www.ncbi.nlm.nih.gov/pubmed/24580845 http://dx.doi.org/10.1186/1824-7288-40-24 |
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author | Stagi, Stefano Losi, Stefania Chiarelli, Francesco de Martino, Maurizio Falcini, Fernanda |
author_facet | Stagi, Stefano Losi, Stefania Chiarelli, Francesco de Martino, Maurizio Falcini, Fernanda |
author_sort | Stagi, Stefano |
collection | PubMed |
description | We describe a girl with Turner syndrome, a genetic disorder of the X chromosome in a phenotypic female at increased risk of autoimmune and immunological diseases, who developed Kawasaki disease at the age of four years. Given the possible relationship between these two disorders, we recommend suspecting Kawasaki disease in patients with Turner syndrome who present with persistent fever of unknown origin and who are not responsive to antibiotic therapy. Attention should be given to this phenomenon, as patients with Turner syndrome are themselves at higher risk of cardiovascular defects. Further studies are needed to better clarify this issue. |
format | Online Article Text |
id | pubmed-3944673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39446732014-03-07 Kawasaki disease in a girl with turner syndrome: a remarkable association Stagi, Stefano Losi, Stefania Chiarelli, Francesco de Martino, Maurizio Falcini, Fernanda Ital J Pediatr Case Report We describe a girl with Turner syndrome, a genetic disorder of the X chromosome in a phenotypic female at increased risk of autoimmune and immunological diseases, who developed Kawasaki disease at the age of four years. Given the possible relationship between these two disorders, we recommend suspecting Kawasaki disease in patients with Turner syndrome who present with persistent fever of unknown origin and who are not responsive to antibiotic therapy. Attention should be given to this phenomenon, as patients with Turner syndrome are themselves at higher risk of cardiovascular defects. Further studies are needed to better clarify this issue. BioMed Central 2014-02-28 /pmc/articles/PMC3944673/ /pubmed/24580845 http://dx.doi.org/10.1186/1824-7288-40-24 Text en Copyright © 2014 Stagi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Stagi, Stefano Losi, Stefania Chiarelli, Francesco de Martino, Maurizio Falcini, Fernanda Kawasaki disease in a girl with turner syndrome: a remarkable association |
title | Kawasaki disease in a girl with turner syndrome: a remarkable association |
title_full | Kawasaki disease in a girl with turner syndrome: a remarkable association |
title_fullStr | Kawasaki disease in a girl with turner syndrome: a remarkable association |
title_full_unstemmed | Kawasaki disease in a girl with turner syndrome: a remarkable association |
title_short | Kawasaki disease in a girl with turner syndrome: a remarkable association |
title_sort | kawasaki disease in a girl with turner syndrome: a remarkable association |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944673/ https://www.ncbi.nlm.nih.gov/pubmed/24580845 http://dx.doi.org/10.1186/1824-7288-40-24 |
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