Volume 16, Issue 56 (Jan 2007)                   J Mazandaran Univ Med Sci 2007, 16(56): 155-160 | Back to browse issues page

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Ghafari J, Ghareh Gozlou M, Nazari Z. Hyper IgE syndrome, a case report. J Mazandaran Univ Med Sci. 2007; 16 (56) :155-160
URL: http://jmums.mazums.ac.ir/article-1-190-en.html
Abstract:   (8584 Views)
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.
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