HRA004688
Title:
Case report: A novel IRF2BP2 mutation in an IEI patient with recurrent infections and autoimmune disorders
Release date:
2023-05-30
Description:
We identified a novel IRF2BP2 mutation in a family with a member diagnosed with IEI. Immune monitoring and WGS as auxiliary tests are helpful in identifying genetic defects and assisting diagnosis in patients with clinically highly suspected immune abnormalities and deficiencies in inflammation regulation. In addition, mNGS techniques allow a more comprehensive assessment of the pathogenic characteristics of these patients. This report further validates the association of IRF2BP2 deficiency and IEI, and expands IEI phenotypes.
Data Accessibility:   
Open access
BioProject:
Study type:
Disease Study
Disease name:
common variable immunodeficiency
Individuals & samples
Files
Submitter:   ji yuan / ji.yuan@zs-hospital.sh.cn
Organization:   Zhongshan Hospital, Fudan University
Submission date:   2023-05-19