JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, vol.138, no.1, pp.241-251, 2016 (SCI-Expanded)
Background: Chronic granulomatous disease (CGD) is a rare primary immunodeficiency caused by inborn errors of the phagocyte nicotinamide adenine dinucleotide phosphate oxidase complex. From the first year of life onward, most affected patients display multiple, severe, and recurrent infections caused by bacteria and fungi. Mycobacterial infections have also been reported in some patients.