Results 31 to 40 of about 64,916 (281)
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].
D, Goldblatt, A J, Thrasher
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Chronic Granulomatous Disease Associated with Chronic Glomerulonephritis [PDF]
, 1985 A boy with chronic granulomatous disease (CGD) developed glomerulonephritis at the age of 12 years. The glomerulonephritis progressed to terminal uraemia at age 15 when maintenance haemodialysis was started.
J. J. FRIFELT +9 more
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Recent advances in chronic granulomatous disease
Genes and Diseases, 2020 Chronic granulomatous disease (CGD) is an inherited defect of phagocyte function due to defective NADPH oxidase. Patients with CGD are not able to effectively clear the infections because of the defect in the phagocyte production of oxygen free radicals ...
Gummadi Anjani +6 more
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Frontiers in Medicine, 2021 Uveitis associated with Vogt-Koyanagi-Harada (VKH) disease is a bilateral, chronic, granulomatous autoimmune disease associated with vitiligo, poliosis, alopecia, and meningeal and auditory manifestations.
Ahmed M. Abu El-Asrar +4 more
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Gene symbol: CYBB. Disease: X-linked chronic granulomatous disease. [PDF]
, 2005 International audienceThe X-linked chronic granulomatous disease is caused by a defect in CYBB gene encoding the large subunit of cytochrome b558, also called ...
Stasia, M. J.
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Indian Journal of Dermatology, Venereology and Leprology, 2005 A 2(1/2)-year-old child presented with multiple discrete granulomatous lesions on the face and flexural regions since the age of 2 months along with lymphadenopathy. The patient also had recurrent bouts of pyodermas and respiratory tract infections.
Pradeep S, Nair +4 more
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Chronic granulomatous disease mimicking early-onset Crohn's disease with cutaneous manifestations [PDF]
, 2014 Background: Chronic granulomatous disease is a rare inherited disorder of the innate immune system. In patients with a clinical history of recurrent or persistent infections, especially infections caused by uncommon species, chronic granulomatous disease
DUSE, MARZIA +8 more
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Recurrent Hypothermia and Autonomic Dysfunction Secondary to Shapiro Syndrome
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT A 44‐year‐old man presented with recurrent hypothermia, diaphoresis and hypertension. Extensive investigation for infectious, inflammatory, metabolic and endocrine aetiologies was negative. MR scan of the brain demonstrated no lesions but revealed callosal dysgenesis, consistent with Shapiro syndrome.
Naveen Kumar +3 more
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Case Report - Chronic granulomatous disease [PDF]
, 2005 A 2½-year-old child presented with multiple discrete granulomatous lesions on the face and flexural regions since the age of 2 months along with lymphadenopathy.
Prasanna K. Moorthy +4 more
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Self-inactivating gammaretroviral vectors for the gene therapy of chronic granulomatous disease [PDF]
, 2008 Chronic granulomatous disease (CGD) is a rare inherited primary immunodeficiency characterized by defective intracellular oxidative killing of ingested invading microbes by PMN and monocytes.
Moreno Carranza, Bibiana
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