| Literature DB >> 28318195 |
Alicia Montaner Ramón1, Laura Murillo Sanjuán2, Cristina Martínez Faci2, Carmelo Guerrero Laleona2, Carmen Rodríguez-Vigil Iturrate2.
Abstract
Chronic granulomatous disease (CGD) is a primary immunodeficiency with an incidence of 1/200,000-250,000 live births. CGD affects mainly male patients, most of the mutations being X-linked, and autosomal recessive forms occur more frequently in communities with greater numbers of consanguineous marriages. CGD is characterized by sensitivity to recurrent and severe bacterial and fungal infections, with formation of granulomas due to the inability of phagocytes to generate reactive oxygen compounds, necessary for the intracellular death of phagocytic microorganisms. We report three cases of CGD in which Serratia marcescens was isolated, and after detailed anamnesis and performance of neutrophil function tests, a molecular diagnosis of the disease was reached. CGD can be manifested in a wide variety of ways, so that high suspicion and a meticulous anamnesis are essential to reach a diagnosis. Sociedad Argentina de Pediatría.Entities:
Keywords: Serratia marcescens; granuloma; pediatrics; phagocytes; primary immunodeficiencies
Mesh:
Year: 2017 PMID: 28318195 DOI: 10.5546/aap.2017.e108
Source DB: PubMed Journal: Arch Argent Pediatr ISSN: 0325-0075 Impact factor: 0.635