Report of one case of hyperimmunoglobulin E syndrome

Author(s):
Mohammad AminianfarMohammad Aminianfar1,*, aliasghar saedialiasghar saedi1, mohammad darvishimohammad darvishi1
1Assistant Professor of Infectious and Tropical disease, Army University of Medical Sciences, Tehran, Iran.
*Corresponding Author: Assistant Professor of Infectious and Tropical disease, Army University of Medical Sciences, Tehran, Iran. Email: [email protected]

Zahedan Journal of Research in Medical Sciences:Vol. 13, issue 5; e93920
Published online:May 19, 2011
Article type:Case Report
Received:Nov 16, 2010
Accepted:Oct 17, 2010
How to Cite:Aminianfar M, saedi A, darvishi M. Report of one case of hyperimmunoglobulin E syndrome. Zahedan J Res Med Sci. 2011;13(5):e93920. doi:

Abstract

Hyperimmunoglobulin E (HIE) syndrome is a rare immunodeficiency disorder. HIE syndrome has multiple abnormalities include recurrent skin abscesses (hence, the name Job syndrome), pneumonia, high serum levels of IgE, Facial, dental and skeletal features. We presented a case of HIE with dermatologic findings, recurrent productive cough and facial features. The diagnosis of HIE require differentiation from other disease. No definitive therapy is available for the treatment. The mainstay of treatment is the control of bacterial infections.

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Copyright

© 2011, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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