Partial and Transient Clinical Response to Omalizumab in IL-21-Induced Low STAT3-Phosphorylation on Hyper-IgE Syndrome

Hyper-IgE syndrome (HIES) is a rare primary immunodeficiency characterized by elevated levels of immunoglobulin E (IgE), eczematous dermatitis, cold abscesses, and recurrent infections of the lung and skin caused by Staphylococcus aureus. The dominant form is characterized by nonimmunologic features...

Descripción completa

Detalles Bibliográficos
Autores principales: Alonso-Bello, Cesar Daniel, Jiménez-Martínez, María del Carmen, Vargas-Camaño, María Eugenia, Hierro-Orozco, Sagrario, Ynga-Durand, Mario Alberto, Berrón-Ruiz, Laura, Alcántara-Montiel, Julio César, Santos-Argumedo, Leopoldo, Herrera-Sánchez, Diana Andrea, Lozano-Patiño, Fernando, Castrejón-Vázquez, María Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637684/
https://www.ncbi.nlm.nih.gov/pubmed/31355024
http://dx.doi.org/10.1155/2019/6357256

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637684/
https://www.ncbi.nlm.nih.gov/pubmed/31355024
http://dx.doi.org/10.1155/2019/6357256

Ejemplares similares