Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: Report of three new mutations

被引:24
作者
Bachrach, BE
Weinstein, DA
Orho-Melander, M
Burgess, A
Wolfsdorf, JI
机构
[1] Childrens Hosp, Div Endocrinol, Boston, MA 02115 USA
[2] Childrens Hosp Dartmouth, Manchester, NH USA
[3] Dartmouth Coll Sch Med, Manchester, NH USA
[4] Lund Univ, Wallenberg Lab, Dept Endocrinol, Malmo, Sweden
[5] Harvard Univ, Sch Med, Boston, MA USA
关键词
D O I
10.1067/mpd.2002.124317
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Although glycogen storage disease type 0 (GSD0) is included in the differential diagnosis of ketotic hypoglycemia, it usually is not considered in the evaluation of glucosuria or hyperglycemia. We describe two children with GSD0, confirmed by mutation analysis, who had glucosuria and hyperglycemia. Because of the variable presentation of this disorder and previous dependence on liver biopsy to confirm diagnosis, it is likely that GSD0 is underdiagnosed.
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收藏
页码:781 / 783
页数:3
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