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Article

Health-Related Quality of Life in 91 Patients with X-Linked Agammaglobulinemia.

Journal of clinical immunology - 1 May 2022

Altman Katherine, Zhou Chuan, Hernandez-Trujillo Vivian, Scalchunes Christopher, Rawlings David J, de la Morena M Teresa

Abstract excerpt

PURPOSE: X-linked agammaglobulinemia (XLA) is a primary immunodeficiency (PID) caused by a defect in the gene encoding for Bruton tyrosine kinase (BTK). In the absence of a functional BTK, patients have low or absent circulating B cells and low or absent serum immunoglobulin. Despite gammaglobulin replacement and prompt use of antimicrobial agents, patients with XLA continue to experience infectious and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 35284987
DOI: 10.1007/s10875-022-01222-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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