Chronic granulomatous disease; Three different clinical presentation
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Dosyalar
Tarih
2017
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
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Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Chronic 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.
Açıklama
Anahtar Kelimeler
Kaynak
Annals of Medical Research
WoS Q DeÄŸeri
Scopus Q DeÄŸeri
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Künye
Halil 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/2182
