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Clinical, Immunological, and Molecular Findings of Patients with p47

Authors :
Manasi, Kulkarni
Mukesh, Desai
Maya, Gupta
Aparna, Dalvi
Prasad, Taur
Antony, Terrance
Sunil, Bhat
Mamta, Manglani
Revathi, Raj
Ira, Shah
Manisha, Madkaikar
Source :
Journal of clinical immunology. 36(8)
Publication Year :
2016

Abstract

Chronic granulomatous disease (CGD) is a group of inherited disorder of phagocytes, resulting from mutations in the components of the NADPH oxidase complex. Reduced or absent oxygen radical synthesis seen in these patients leads to impaired killing of intracellular bacteria and fungi. CGD clinically presents with recurrent and life-threatening infections as well as granulomatous inflammatory responses. p47

Details

ISSN :
15732592
Volume :
36
Issue :
8
Database :
OpenAIRE
Journal :
Journal of clinical immunology
Accession number :
edsair.pmid..........f8c081d107b782727ccb1703ad2a5afa