| Literature DB >> 26472314 |
Glynis Frans1, Leen Moens1, Rik Schrijvers2, Greet Wuyts1, Bernard Bouckaert3, Heidi Schaballie4,5, Lieven Dupont6, Xavier Bossuyt1,7, Anniek Corveleyn8, Isabelle Meyts9,10.
Abstract
Autosomal recessive IL-1R-associated kinase 4 (IRAK-4) deficiency is a rare cause of recurrent pyogenic infections with limited inflammatory responses. We describe an adult female patient with severe lung disease who was phenotypically diagnosed as suffering from autosomal dominant Hyper IgE syndrome (AD HIES) because of recurrent skin infections with Staphylococcus aureus, recurrent pneumonia and elevated serum IgE levels. In contrast to findings in AD HIES patients, no abnormalities were found in the Th17 and circulating follicular helper T cell subsets. A panel-based sequencing approach led to the identification of a homozygous IRAK4 stop mutation (c.877C > T, p.Gln293*).Entities:
Keywords: IRAK-4; Primary immunodeficiency; hyper IgE syndrome; next-generation sequencing
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Year: 2015 PMID: 26472314 DOI: 10.1007/s10875-015-0205-x
Source DB: PubMed Journal: J Clin Immunol ISSN: 0271-9142 Impact factor: 8.317