HYPER IGE SYNDROME: A CASE REPORT

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GHAFARI JAVAD; GHARAHGOUZLOU M.; NAZARI ZEYNAB

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Paper Information

Journal: Journal of Mazandaran University of Medical Sciences Year:2007 | Volume:16 | Issue:56 Page(s): 155-160

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Information Journal Paper

Title

HYPER IGE SYNDROME: A CASE REPORT

Author(s)

GHAFARI JAVAD | GHARAHGOUZLOU M. | NAZARI ZEYNAB | Issue Writer Certificate

Keywords

HYPER IGEQ3

JOB'S SYNDROMEQ3

PNEUMATOCELEQ3

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.

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APA: Copy

GHAFARI, JAVAD, GHARAHGOUZLOU, M., & NAZARI, ZEYNAB. (2007). HYPER IGE SYNDROME: A CASE REPORT. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, 16(56), 155-160. SID. https://sid.ir/paper/45636/en

Vancouver: Copy

GHAFARI JAVAD, GHARAHGOUZLOU M., NAZARI ZEYNAB. HYPER IGE SYNDROME: A CASE REPORT. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2007;16(56):155-160. Available from: https://sid.ir/paper/45636/en

IEEE: Copy

JAVAD GHAFARI, M. GHARAHGOUZLOU, and ZEYNAB NAZARI, “HYPER IGE SYNDROME: A CASE REPORT,” JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, vol. 16, no. 56, pp. 155–160, 2007, [Online]. Available: https://sid.ir/paper/45636/en

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