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...

Descripción completa

Detalles Bibliográficos
Autores principales: Szczawinska-Poplonyk, Aleksandra, Kycler, Zdzislawa, Pietrucha, Barbara, Heropolitanska-Pliszka, Edyta, Breborowicz, Anna, Gerreth, Karolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Review
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

Internet

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

Ejemplares similares