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Chronic granulomatous disease presenting with hypogammaglobulinemia
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نویسنده
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hanoglu d. ,özgür t. ,ayvaz d. ,köker m. ,sanal ö.
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منبع
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journal of investigational allergology and clinical immunology - 2011 - دوره : 21 - شماره : 4 - صفحه:310 -312
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چکیده
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Chronic granulomatous disease (cgd) is a primary immunodefi ciency disorder caused by inherited defects in the nicotinamide adenine dinucleotide phosphate oxidase complex. the neutrophils of patients with cgd can ingest bacteria normally,but the oxidative processes that lead to superoxide anion formation,hydrogen peroxide production,nonoxidative pathway activation,and bacterial killing are impaired. serious infections result from microorganisms that produce catalase. immunoglobulin levels of patients with cgd are usually normal or elevated. we describe a patient with cgd associated with hypogammaglobulinemia,an unusual co-occurrence. © 2011 esmon publicidad.
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کلیدواژه
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B-cell subsets; Chronic granulomatous disease (CGD); Hypogammaglobulinemia; Memory b cell
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آدرس
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hacettepe university,faculty of medicine,ankara, Turkey, division of immunology,hacettepe university,ihsan doǧramaci childrens hospital,ankara, Turkey, division of immunology,hacettepe university,ihsan doǧramaci childrens hospital,ankara, Turkey, division of immunology,diskapi children's hospital,ankara, Turkey, division of immunology,hacettepe university,ihsan doǧramaci childrens hospital,ankara, Turkey
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Authors
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