Pediatr Allergy Respir Dis.  2002 Dec;12(4):328-333.

A Case of X-Linked Agammaglobulinemia Associated with Severe Neutropenia

Affiliations
  • 1Department of Pediatics, College of Medicine, Dankook University, Cheonan, Korea. milee@asthmacamp.pe.kr
  • 2Department of Pediatics, College of Medicine, Chungnam National University, Taejon, Korea.

Abstract

X-linked agammaglobulinemia(XLA) is characterized by markedly reduced number of B lymphocytes, panhypogammaglobulinemia, recurrent bacterial infections in the first few years of life because of genetic defect for Bruton's tyrosine kinase at Xq22 region. Although XLA is a typical humoral immunodeficiency disease, severe neutropenia is sometimes presented in acute infection phase. We report a 23-month-boy with XLA who presented prolonged pneumonia, severe neutropenia over one month and profound panhypogammaglobulinemia. As his pneumonia improved, neutropenia subsided, but panhypogammaglobulinemia sustained. He was confirmed to have a point mutation in Btk-gene by direct-sequencing of Btk-gene.

Keyword

X-Linked agammaglobulinemia; Neutropenia

MeSH Terms

Agammaglobulinemia*
B-Lymphocytes
Bacterial Infections
Neutropenia*
Pneumonia
Point Mutation
Protein-Tyrosine Kinases
Protein-Tyrosine Kinases
Full Text Links
  • PARD
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr