翻訳と辞書
Words near each other
・ Glycobiology (journal)
・ Glycobius
・ Glycocalyx
・ Glycochenodeoxycholate sulfotransferase
・ Glycochenodeoxycholic acid
・ Glycocholic acid
・ Glycoconjugate
・ Glycocyamine
・ Glycodeoxycholic acid
・ Glycogen
・ Glycogen body
・ Glycogen branching enzyme
・ Glycogen debranching enzyme
・ Glycogen phosphorylase
・ Glycogen phosphorylase isoenzyme BB
Glycogen storage disease
・ Glycogen storage disease type 0
・ Glycogen storage disease type I
・ Glycogen storage disease type II
・ Glycogen storage disease type III
・ Glycogen storage disease type IV
・ Glycogen storage disease type IX
・ Glycogen storage disease type V
・ Glycogen storage disease type VI
・ Glycogen storage disease type XI
・ Glycogen synthase
・ Glycogen synthase kinase
・ Glycogen-branching enzyme deficiency
・ Glycogenase
・ Glycogenesis


Dictionary Lists
翻訳と辞書 辞書検索 [ 開発暫定版 ]
スポンサード リンク

Glycogen storage disease : 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)
ウィキペディアで「Glycogen storage disease」の詳細全文を読む



スポンサード リンク
翻訳と辞書 : 翻訳のためのインターネットリソース

Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.