| Literature DB >> 27867589 |
Yuanda Xu1, Qi Qing1, Xuesong Liu1, Sibei Chen1, Ziyi Chen2, Xuefeng Niu1, Yaxia Tan1, Weiqun He1, Xiaoqing Liu1, Yimin Li1, Rongchang Chen1, Ling Chen3.
Abstract
X-linked agammaglobulinemia (XLA) is caused by mutation in the gene coding for Bruton's tyrosine kinase (BTK), which impairs peripheral B cell maturation and hypogammaglobulinemia. In this report, we present a case of XLA in a 22-year-old adult male. Genetic testing revealed a novel mutation located at the conserved region (c.383T>C). The patient had a history of recurrent respiratory tract infection which eventually progressed to chronic type II respiratory failure. Several pathogenic bacteria were isolated on culture of respiratory secretions obtained on bronchoscopy. The patient improved on treatment with antibiotics.Entities:
Keywords: X-linked agammaglobulinemia (XLA); novel mutation
Year: 2016 PMID: 27867589 PMCID: PMC5107543 DOI: 10.21037/jtd.2016.10.12
Source DB: PubMed Journal: J Thorac Dis ISSN: 2072-1439 Impact factor: 2.895