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Immunological parameters in girls with Turner syndrome

Disturbances in the immune system has been described in Turner syndrome, with an association to low levels of IgG and IgM and decreased levels of T- and B-lymphocytes. Also different autoimmune diseases have been connected to Turner syndrome (45, X), thyroiditis being the most common. Besides the ty...

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Autores principales: Stenberg, Annika E, Sylvén, Lisskulla, Magnusson, Carl GM, Hultcrantz, Malou
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC538258/
https://www.ncbi.nlm.nih.gov/pubmed/15563731
http://dx.doi.org/10.1186/1477-5751-3-6
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author Stenberg, Annika E
Sylvén, Lisskulla
Magnusson, Carl GM
Hultcrantz, Malou
author_facet Stenberg, Annika E
Sylvén, Lisskulla
Magnusson, Carl GM
Hultcrantz, Malou
author_sort Stenberg, Annika E
collection PubMed
description Disturbances in the immune system has been described in Turner syndrome, with an association to low levels of IgG and IgM and decreased levels of T- and B-lymphocytes. Also different autoimmune diseases have been connected to Turner syndrome (45, X), thyroiditis being the most common. Besides the typical features of Turner syndrome (short stature, failure to enter puberty spontaneously and infertility due to ovarian insufficiency) ear problems are common (recurrent otitis media and progressive sensorineural hearing disorder). Levels of IgG, IgA, IgM, IgD and the four IgG subclasses as well as T- and B-lymphocyte subpopulations were investigated in 15 girls with Turners syndrome to examine whether an immunodeficiency may be the cause of their high incidence of otitis media. No major immunological deficiency was found that could explain the increased incidence of otitis media in the young Turner girls.
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spelling pubmed-5382582004-12-19 Immunological parameters in girls with Turner syndrome Stenberg, Annika E Sylvén, Lisskulla Magnusson, Carl GM Hultcrantz, Malou J Negat Results Biomed Research Disturbances in the immune system has been described in Turner syndrome, with an association to low levels of IgG and IgM and decreased levels of T- and B-lymphocytes. Also different autoimmune diseases have been connected to Turner syndrome (45, X), thyroiditis being the most common. Besides the typical features of Turner syndrome (short stature, failure to enter puberty spontaneously and infertility due to ovarian insufficiency) ear problems are common (recurrent otitis media and progressive sensorineural hearing disorder). Levels of IgG, IgA, IgM, IgD and the four IgG subclasses as well as T- and B-lymphocyte subpopulations were investigated in 15 girls with Turners syndrome to examine whether an immunodeficiency may be the cause of their high incidence of otitis media. No major immunological deficiency was found that could explain the increased incidence of otitis media in the young Turner girls. BioMed Central 2004-11-25 /pmc/articles/PMC538258/ /pubmed/15563731 http://dx.doi.org/10.1186/1477-5751-3-6 Text en Copyright © 2004 Stenberg 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 cited.
spellingShingle Research
Stenberg, Annika E
Sylvén, Lisskulla
Magnusson, Carl GM
Hultcrantz, Malou
Immunological parameters in girls with Turner syndrome
title Immunological parameters in girls with Turner syndrome
title_full Immunological parameters in girls with Turner syndrome
title_fullStr Immunological parameters in girls with Turner syndrome
title_full_unstemmed Immunological parameters in girls with Turner syndrome
title_short Immunological parameters in girls with Turner syndrome
title_sort immunological parameters in girls with turner syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC538258/
https://www.ncbi.nlm.nih.gov/pubmed/15563731
http://dx.doi.org/10.1186/1477-5751-3-6
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