Autosomal recessive hyper‐IgE syndrome due to DOCK8 deficiency: An adjunctive role for omalizumab

Autosomal recessive hyper‐IgE syndrome due to DOCK8 deficiency: An adjunctive role for omalizumab

Abstract Autosomal recessive hyper‐IgE syndrome (AR‐HIES) is a rare primary immunodeficiency disorder characterized by high serum IgE levels, recurrent viral skin infections, severe allergies, and early‐onset malignancies, associated with mutations in the gene encoding the dedicator of cytokinesis 8...

Full description

Bibliographic Details
Main Authors: Kim Han Nguyen, Quynh Anh Nguyen, Mai Hoang Tran, Thu Thuy Can, Mai Thi Vu, Nam Sy Vo, Hieu Chu Chi, Sheryl vanNunen, Dinh Van Nguyen
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-12-01
Series:Journal of Cutaneous Immunology and Allergy
Subjects:
AR‐HIES
DOCK8 deficiency
immunodeficiency disorder
omalizumab
recurrent viral infection
Online Access:https://doi.org/10.1002/cia2.12273

Internet

https://doi.org/10.1002/cia2.12273

Similar Items