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- Title
Late-Onset Lymphopenia and ITP in a Patient with Hyper IgM Syndrome Due to a Homozygous Variant in AICDA.
- Authors
Adatia, Adil; Ritchie, Bruce
- Abstract
Keywords: Hyper IgM syndrome; AID deficiency; AICDA; primary immunodeficiency; antibody deficiency EN Hyper IgM syndrome AID deficiency AICDA primary immunodeficiency antibody deficiency 1540 1542 3 09/15/23 20231001 NES 231001 To the Editor: Hyper IgM syndromes (HIGM) are rare primary immunodeficiencies characterized by impaired class switch recombination (CSR) often together with defective somatic hypermutation (SHM). Hyper IgM syndrome, AICDA, AID deficiency, primary immunodeficiency, antibody deficiency.
- Subjects
LYMPHOPENIA; INTERSTITIAL lung diseases; COMMON variable immunodeficiency; SYNDROMES; IMMUNOGLOBULIN light chains
- Publication
Journal of Clinical Immunology, 2023, Vol 43, Issue 7, p1540
- ISSN
0271-9142
- Publication type
Article
- DOI
10.1007/s10875-023-01546-z