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Article

[X-linked agammaglobulinemia (XLA) associated with agranulocytosis--case report].

Wiadomosci lekarskie (Warsaw, Poland : 1960) - 1 Jan 2003

Irga Ninela, Wierzba Jolanta, Brozek Jacek, Ochman Karolina, Kanegane Hirokazu, Miyawaki Toshio, Neuman-Łaniec Magdalena

Abstract excerpt

In this case study authors presented the clinical characteristics of X-linked agammaglobulinemia (XLA) associated with agranulocytosis diagnosed in a 2-year-old boy. Affected child lacked circulating mature B cells, presented low levels of serum immunoglobulins, but did not suffer from recurrent bacterial infections. XLA is a primary immunodeficiency caused by a defective tyrosine kinase (Btk) in B cells. Our...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 14969169

Genes

BTK

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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