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Purulent meningitis in X-linked agammaglobulinemia: one case report
Anyi Ba1, Lijiang Wang2, Ruifang Ren3
1Department of Neurology, The Second Affiliated Hospital of Henan Medical University, Xinxiang, Henan, China.
None:
X-linked agammaglobulinemia (XLA) is characterized by a triad of primary immunodeficiency, profound hypogammaglobulinemia due to absent antibody production, and a consequent predisposition to severe and recurrent bacterial infections. We employed next-generation sequencing (NGS) on patients with immunodeficiency and their immediate relatives to facilitate the diagnosis and genetic counseling of XLA, thereby improving our understanding of this rare disorder.
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