Hyper IgE syndrome, a case report

Ghafari, J and GharehGozlou, M and Nazari, Z (2007) Hyper IgE syndrome, a case report. Journal of Mazandaran University of Medical Sciences, 16 (56). pp. 155-160.

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Official URL: http://jmums.mazums.ac.ir/article-1-190-en.html

Abstract

Hyper IgE syndrome (Job�s syndrome) is a primary immunodeficiency disease with recurrent infections especially staphylococcal, coarse face, skeletal abnormality and significant increase in serum IgE level (IgE >2000IU/ml). We present a 16 years old boy admitted with chronic cough, dyspnea, eczema and pneumatocele. He had a history of chronic dermal infection since 1 month after birth. The diagnosis of hyper IgE syndrome was made according to typical history and significant high serum IgE level.

Item Type: Article
Uncontrolled Keywords: Hyper IgE, Job�s syndrome, pneumatocele
Depositing User: Unnamed user with email eprints@mazums.ac.ir
Date Deposited: 04 Jan 2018 17:54
Last Modified: 04 Jan 2018 17:54
URI: http://eprints.mazums.ac.ir/id/eprint/3159

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