翻訳と辞書 Words near each other ・ 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 ・ Glycogenic acanthosis ・ Glycogenin ・ Glycogenin-1 ・ Glycogenolysis ・ Glycoinformatics ・ Glycol cleavage ・ Glycol dehydration ・ Glycol distearate ・ Glycol ethers Dictionary Lists mini英和辞書 mini和英辞書 Webster 1913 Latin-English FOLDOC Wikipedia English ウィキペディア

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 type XI ： ウィキペディア英語版 Glycogen storage disease type XI Glycogen storage disease type XI is a form of glycogen storage disease. It is also known as "Fanconi–Bickel syndrome", for Guido Fanconi and Horst Bickel, who first described it in 1949. It is associated with GLUT2, a glucose transport protein which, when functioning normally, allows glucose to exit several tissues, including the liver, nephrons,and enterocytes of the intestines, and enter the blood. The syndrome results in hepatomegaly secondary to glycogen accumulation, glucose and galactose intolerance, fasting hypoglycaemia, a characteristic proximal tubular nephropathy and severe short stature. ==References== 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 type XI」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.