| Literature DB >> 24064560 |
Francisco Gimenez-Sanchez1, Elena Cobos-Carrascosa, Miguel Sanchez-Forte, Miguel Martinez-Lirola, Encarnacion Lopez-Ruzafa, Rafael Galera-Martinez, Teresa Del Rosal, Teresa Del Rosal-Babes, Monica Martinez-Gallo.
Abstract
Deficiency in the interleukin12/INFgamma pathway is a genetic condition that predisposes to some infections, including nontuberculous mycobacteria infection and extraintestinal salmonellosis. We report 2 cases in sisters who were diagnosed with a genetic defect caused by a new mutation in Interleukin-12 receptor β1 chain (IL12Rβ1) leading to different clinical presentations and responses to therapy.Entities:
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Year: 2014 PMID: 24064560 DOI: 10.1097/INF.0000000000000099
Source DB: PubMed Journal: Pediatr Infect Dis J ISSN: 0891-3668 Impact factor: 2.129