volume 88, issue 5, P836-838 2013
DOI: 10.1590/abd1806-4841.20132112
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Alexandre Moretti de Lima,
Vitor Arantes Sperandio,
Sheila Pereira da Rocha
et al.

Abstract: 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.

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