| Autor: |
J. Ghafari, M. Ghareh Gozlou, Z. Nazari |
| Jazyk: |
angličtina |
| Rok vydání: |
2007 |
| Předmět: |
|
| Zdroj: |
Journal of Mazandaran University of Medical Sciences, Vol 16, Iss 56, Pp 155-160 (2007) |
| ISSN: |
1735-9260 |
| Popis: |
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. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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