Mother and daughter carrying the same KCNJ11 mutation but with a different response to switching from insulin to sulfonylurea

被引：7
|
作者：
Russo, Chiara [1 ]
Salina, Alessandro [1 ]
Aloi, Concetta [1 ]
Iafusco, Dario [2 ]
Lorini, Renata [1 ]
d'Annunzio, Giuseppe [1 ]
机构：
[1] Univ Genoa, Pediat Clin, IRCCS G Gaslini Inst, I-16147 Genoa, Italy
[2] Univ Naples 2, Dept Pediat, Naples, Italy
来源：
DIABETES RESEARCH AND CLINICAL PRACTICE | 2011年 / 94卷 / 02期
关键词：
Sulfonylureas; Switch to SU; PNDM treatment; KCNJ11; ACTIVATING MUTATIONS; DIABETES-MELLITUS; KIR6.2; INSIGHTS; GENES;
D O I：
10.1016/j.diabres.2011.07.039
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
KCNJ11 gene mutations are related to permanent neonatal diabetes mellitus (PNDM). Glycemic stability minimizes the risk of complications. Sulfonylureas (SU) are the proven best therapeutic option. We report a 18-month follow-up of switching from insulin to SU in a mother and her daughter with PNDM due to KCNJ11 mutation. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码：E50 / E52
页数：3
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