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| Glycogen storage diseases ： ウィキペディア英語版 |
Glycogen storage disease
Glycogen storage disease (GSD, also glycogenosis and dextrinosis) is the result of defects in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types.
GSD has two classes of cause: genetic and acquired. Genetic GSD is caused by any inborn error of metabolism (genetically defective enzymes) involved in these processes. In livestock, acquired GSD is caused by intoxication with the alkaloid castanospermine.
== Prevalence ==
Overall, according to a study in British Columbia, approximately 2.3 children per 100 000 births (1 in 43,000) have some form of glycogen storage disease. In the United States, they are estimated to occur in 1 per 20,000-25,000 births.〔(eMedicine Specialties > Glycogen-Storage Disease Type I ) Author: Karl S Roth. Updated: Aug 31, 2009〕 A Dutch study estimated it to be 1 in 40,000.
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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