Chronic granulomatous disease; Three different clinical presentation

dc.contributor.authorCeliksoy, Mehmet Halil
dc.contributor.authorKoker, Mustafa Yavuz
dc.contributor.authorSensoy, Gulnar
dc.contributor.authorCeyhan, Meltem
dc.contributor.authorBelet, Nursen
dc.contributor.authorYildiran, Alisan
dc.date.accessioned2022-02-16T13:15:44Z
dc.date.available2022-02-16T13:15:44Z
dc.date.issued2017
dc.departmentİnönü Üniversitesien_US
dc.description.abstractChronic granulomatous disease is an inherited disorder of nicotinamide-adenine dinucleotide phosphate oxidase and results in a defect in intracellular killing of ingested microorganisms characterized by recurrent life threatening bacterial and fungal infections. The disease is classified by mutations in specific subunits of the NADPH oxidase enzyme. There are one X-linked and four autosomal recessive forms of disease. The organisms cultured from lesion of patients with chronic granulomatous disease are generally catalase-producing including Staphylococci, Escherichia coli, Serratia; or fungi such as Aspergillus species. Recurrent or serious infections usually lead to diagnosis of disease in early childhood. We report three male patients who were diagnosed 5, 10, 13 years old, respectively and showed different clinical presentation.en_US
dc.identifier.citationHalil Celiksoy, M., Yavuz Koker, M., Sensoy, G., Belet, N., Ceyhan, M., & Yildiran, A. (2021). Chronic granulomatous disease; Three different clinical presentation . Annals of Medical Research, 24(2), 0214–0217. Retrieved from https://annalsmedres.org/index.php/aomr/article/view/2182en_US
dc.identifier.urihttps://hdl.handle.net/11616/47319
dc.language.isoenen_US
dc.relation.ispartofAnnals of Medical Researchen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleChronic granulomatous disease; Three different clinical presentationen_US
dc.typeArticleen_US

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