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chronic granulomatous disease : ウィキペディア英語版
chronic granulomatous disease

Chronic granulomatous disease (CGD) (also known as Bridges–Good syndrome, Chronic granulomatous disorder, and Quie syndrome) is a diverse group of hereditary diseases in which certain cells of the immune system have difficulty forming the reactive oxygen compounds (most importantly the superoxide radical due to defective phagocyte NADPH oxidase) used to kill certain ingested pathogens.〔(【引用サイトリンク】title=Chronic Granulomatous Disease: Immunodeficiency Disorders: Merck Manual Professional )〕 This leads to the formation of granulomata in many organs. CGD affects about 1 in 200,000 people in the United States, with about 20 new cases diagnosed each year.
This condition was first discovered in 1950 in a series of 4 boys from Minnesota, and in 1957 was named "a fatal granulomatosus of childhood" in a publication describing their disease. The underlying cellular mechanism that causes chronic granulomatous disease was discovered in 1967, and research since that time has further elucidated the molecular mechanisms underlying the disease. Bernard Babior made key contributions in linking the defect of superoxide production of white blood cells, to the etiology of the disease. In 1986, the X-linked form of CGD was the first disease for which positional cloning was used to identify the underlying genetic mutation.
==Classification==

Chronic granulomatous disease is the name for a genetically heterogeneous group of immunodeficiencies. The core defect is a failure of phagocytic cells to kill organisms that they have engulfed because of defects in a system of enzymes that produce free radicals and other toxic small molecules. There are several types, including:
* X-linked chronic granulomatous disease]] (CGD)
* autosomal recessive cytochrome b-negative CGD
* autosomal recessive cytochrome b-positive CGD type I
* autosomal recessive cytochrome b-positive CGD type II
* atypical granulomatous disease

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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