Abstract
A patient is described who had many features of chronic granulomatous disease of childhood, including life-long history of illness, simultaneous granulomatous and purulent response to an organism of low-grade virulence, presence of “golden histiocytes” in the affected organs, and faulty bactericidal capacity of phagocytes. Differing from the classically described cases were his long survival and the absence of evidence of a sex-linked genetic pattern.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
