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dc.contributor.authorDang Mai Lien-
dc.contributor.authorLe Thi Hong Hanh-
dc.contributor.authorTrinh Thi Dung-
dc.date.accessioned2022-11-04T04:02:24Z-
dc.date.available2022-11-04T04:02:24Z-
dc.date.issued2020-
dc.identifier.urihttp://thuvienso.thanglong.edu.vn//handle/TLU/4446-
dc.description.abstractChronic granulomatous disease (CGD) is an inherited primary immunodeficiency disease which is one kind of the phagocytic dysfunction. It is accounted for 1 : 200000 live births in the United States. The mechanism of CGD is mutation in any structural molecules of Nicotinamid Adenine Dinucleotide Phosphate (NADPH) oxidase. Therefore, CGD increases the body’s susceptibility to infections caused by bacteria and fungi with granulomas formed at the sites of infection or inflammation. We report 4 cases diagnosed as suspected CGD in patients suffering from persistent pneumonia in the respiratory unit in Vietnam National Children’s Hospital to recommend colleagues not to mis-diagnose CGD in recurrent or persistent pneumonia.vi_VN
dc.language.isoenvi_VN
dc.publisherJournal of Medical Researchvi_VN
dc.relation.ispartofseries136 (12);-
dc.subjectchronic granulomatous diseasevi_VN
dc.subjectpersistent pneumoniavi_VN
dc.title4 cases from suspected chronic granulomatous disease in the respiratory unit in Vietnam national children's hospitalvi_VN
dc.typemagazinevi_VN
Appears in CollectionsLĩnh vực Khoa học sức khỏe

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