نتایج جستجو برای: chronic granulomatous disease cgd

تعداد نتایج: 1773487  

2010
Masoud Mohammadpour Setareh Mamishi Mahsa Oaji Zahra Pourpak Nima Parvaneh

BACKGROUND Chronic granulomatous disease (CGD) is an immunodeficiency affecting phagocytic leukocytes. Defective respiratory burst mechanism renders the affected patients to be susceptible to catalase positive microorganisms. With the great successes in antibacterial prophylaxis and therapy, fungal infections are a persistent problem. Invasive aspergillosis is the most important cause of mortal...

Journal: :Journal of investigational allergology & clinical immunology 2011
D Hanoglu T T Ozgür D Ayvaz M Y Köker O Sanal

Chronic granulomatous disease (CGD) is a primary immunodeficiency disorder caused by inherited defects in the nicotinamide adenine dinucleotide phosphate oxidase complex. The neutrophils of patient 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 im...

2015
Farid Imanzade Aliakbar Sayarri Pantea Tajik

Chronic Granulomatous Disease (CGD) is an inherited primary immunodeficiency disease which increases the body's susceptibility to infections caused by certain bacteria and fungi. CGD is a rare disease, caused by four genes, one type is 1X linked and the other three are "autosomal recessive". Although clinical presentation is variable, but characteristic features are recurrent pneumonia, lymphad...

Journal: :Journal of Korean Medical Science 1997
M. Kim J. H. Shin S. P. Suh D. W. Ryang C. S. Park C. Kim H. Kook J. Kim

Aspergillus nidulans is one of the several species of Aspergillus with low pathogenicity. The significant infections of A. nidulans in human have rarely been reported, almost exclusively in patients with chronic granulomatous disease (CGD). CGD is a primary immunodeficiency disease which results from the absence of the NADPH oxidase in the phagocytic cells, leading to recurrent pyogenic infecti...

Journal: :Clinical and experimental rheumatology 2007
J Brunner G Dockter A Rösen-Wolff J Roesler

BACKGROUND Chronic granulomatous disease (CGD) is caused by mutations in genes encoding nicotinamide dinucleotide phosphate (NADPH) oxidase subunits. CASE REPORT A boy was diagnosed as having juvenile sarcoidosis because he presented with cervical and pulmonary lymphadenopathy with epitheloid cells and granuloma formation and high angiotensin converting enzyme. Later, a liver abscess was diag...

Journal: :Diagnostic and interventional radiology 2017
Minah Lee Mu Sook Lee Jeong Sub Lee Su Yeon Ko Sun Young Jeong

The purpose of this pictorial essay is to present and summarize findings of various images of chronic granulomatous disease (CGD). CGD represents a heterogeneous group of disorders caused by defective generation of respiratory bursts in human phagocytes. This defect results in abnormal phagocytic functions and defective killing of bacteria by phagocytes. CGD may involve many organs and present ...

Journal: :International Journal of Advances in Pharmacy and Biotechnology 2019

Journal: :The Turkish journal of pediatrics 2015
Aytaç Yaman Zarife Kuloğlu Figen Doğu Aydan İkincioğulları Arzu Ensari Ergin Çiftçi Aydan Kansu

Chronic granulomatous disease (CGD) is an autosomal recessive or X-linked disorder caused by NADPH oxidase deficiency leading to an impaired ability of reactive superoxide anion and metabolite formation and recurring severe bacterial and fungal infections, with a high mortality rate. Diarrhea, colitis, ileus, perirectal abscess formation and anal fissures are reported gastrointestinal findings ...

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