Results 11 to 20 of about 1,240,530 (301)
Indian Journal of Rheumatology, 2020 Common variable immune deficiency (CVID) is a primary immunodeficiency syndrome, characterized by a defective B cell function. Although there is no age or gender predilection, it is usually diagnosed between the second and fourth decades of life.
Veena Shamsudeen +4 more
semanticscholar +1 more source
Pigmentary keratitis and mixed chromatophoroma in a betta fish (Betta splendens)
Aquaculture, Fish and Fisheries, Volume 2, Issue 6, Page 587-592, December 2022., 2022 Graphical Abstract This clinical case report describes a <1 year old betta fish that developed pigmentary keratitis, anterior uveitis, and a mixed chromatophoroma that led to the patient's death. A review of available anecdotal and scientific literature suggests that there may have been a genetic cause for these health problems.
Alicia McLaughlin +3 more
wiley +1 more source
International Forum of Allergy &Rhinology, Volume 13, Issue 1, Page 15-24, January 2023., 2023 Abstract Background Patients with chronic rhinosinusitis (CRS) may have persistence of polyps, discharge, or edema after endoscopic sinus surgery (ESS). Inflammation in CRS can be classified into three endotypes, with the presence of polyps associated with the type 2 endotype.
Eli Stein +12 more
wiley +1 more source
Chronic granulomatous disease [PDF]
The British Journal of Radiology, 1970 Abstract Chronic granulomatous disease is a hereditable disorder in which polymorphs show diminished capacity for killing bacteria. Defective bactericidal activity results in protracted infection. The lesions of chronic granulomatous disease may affect all systems of the body.
A. R. Chrispin, J. Sutcliffe
openaire +6 more sources
Blood, 2020 Chronic Granulomatous Disease (CGD) is a primary immunodeficiency resulting in life-threatening infections and inflammatory complications. Allogeneic hematopoietic cell transplantation (allo-HCT) can cure patients, but indication to transplant remains ...
R. Chiesa +39 more
semanticscholar +1 more source
Clinical observation of Сhronic granulomatous disease in a 6-year-old child
Детские инфекции (Москва), 2020 Chronic granulomatous disease (CGD) is a hereditary disease caused by a genetic defect of violations of oxygen — dependent mechanisms of phagocytosis.
G. A. Kharchenko, O. G. Kimirilova
doaj +1 more source
Journal of Cutaneous Immunology and Allergy, Volume 5, Issue 6, Page 236-237, December 2022., 2022 Patch granuloma annulare is a rare type of granuloma annulare. Histopathologically, patch granuloma annulare shows interstitial infiltration of histiocytes. In our case, immunohistochemical analyses demonstrated CD68‐negative, CD163‐positive M2 macrophages infiltration in an interstitial pattern.
Kenta Ikeda +3 more
wiley +1 more source
Chronic granulomatous disease [PDF]
Clinical and Experimental Immunology, 2000 A clinical syndrome characterized by recurrent life-threatening Staphylococcus aureus, Proteus or Pseudomonas, hypergammaglobulinaemia, and widespread chronic granulomatous infiltration was first recognized in the paediatric literature between 1954 and 1960 [1–3].
Adrian J. Thrasher, David Goldblatt
openaire +2 more sources
Chronic granulomatous disease [PDF]
Pediatric Radiology, 2010 Chronic granulomatous disease (CGD) is a rare congenital immunodeficiency characterized by recurrent bacterial and fungal infections as well as granuloma formation. The manifestations of this disease can involve single or multiple organ systems. The lungs are the most commonly affected organ; however, lymphatic, hepatic, skeletal, gastrointestinal ...
Alexander J. Towbin, Ian J. Chaves
openaire +4 more sources
Chronic Granulomatous Disease: the Experience of Diagnosis and Treatment in Children
Zdorovʹe Rebenka, 2013 Chronic granulomatous disease — primary immunodeficiency with X-linked and autosomal recessive inheritance, characterized by impaired bactericidal function of phagocytic immune system.
L.I. Chernyshova +4 more
doaj +1 more source