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The hyperimmunoglobulin E syndrome - clinical manifestation diversity in primary immune deficiency
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 classical hyper-IgE syndrome which i...
Autores principales: | Szczawinska-Poplonyk, Aleksandra, Kycler, Zdzislawa, Pietrucha, Barbara, Heropolitanska-Pliszka, Edyta, Breborowicz, Anna, Gerreth, Karolina |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226432/ https://www.ncbi.nlm.nih.gov/pubmed/22085750 http://dx.doi.org/10.1186/1750-1172-6-76 |
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