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The hyperimmunoglobulin E syndrome - clinical manifestation diversity in primary immune deficiency
<p>Abstract</p> <p>The hyper-IgE syndromes are rare, complex primary immunodeficiencies characterized by clinical manifestation diversity, by particular susceptibility to staphylococcal and mycotic infections as well as by a heterogeneous genetic origin. Two distinct entities - the...
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| Główni autorzy: | , , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
BMC
2011-11-01
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| Seria: | Orphanet Journal of Rare Diseases |
| Dostęp online: | http://www.ojrd.com/content/6/1/76 |
| Etykiety: |
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