| Autor: |
Lima AM; Federal University of Mato Grosso do Sul, Campo GrandeMS, Brazil., Sperandio VA, Rocha SP, Ribeiro BM, Reis CM |
| Jazyk: |
angličtina |
| Zdroj: |
Anais brasileiros de dermatologia [An Bras Dermatol] 2013 Sep-Oct; Vol. 88 (5), pp. 836-8. |
| DOI: |
10.1590/abd1806-4841.20132112 |
| Abstrakt: |
The hyperimmunoglobulin E syndrome, or Job's syndrome is a rare primary immunodeficiency characterized by recurrent skin abscesses, recurrent respiratory tract infections, and high levels of IgE, eosinophilia, bone and dental changes. We report the case of a fourteen-year-old male patient presenting this disease, with both typical and also some relatively sporadic manifestations. We performed a literature review on the syndrome and its associated clinical findings. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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