Hyper IgE syndrome, a case report
Author(s):
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.
Keywords:
Language:
Persian
Published:
Journal of Mazandaran University of Medical Sciences, Volume:16 Issue: 56, 2007
Page:
155
https://www.magiran.com/p412368
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