A Novel De Novo Missense Mutation in HNF4A Resulting in Sulfonylurea-Responsive Maturity-onset Diabetes of the Young

被引:1
|
作者
Acar, Sezer [1 ]
Abaci, Ayhan [1 ]
Demir, Korcan [1 ]
Ozdemir, Taha Resid [2 ]
Ozyilmaz, Berk [2 ]
Bober, Ece [1 ]
机构
[1] Dokuz Eylul Univ, Fac Med, Dept Pediat, Div Pediat Endocrinol, Izmir, Turkey
[2] Univ Hlth Sci, Izmir Tepecik Training & Res Hosp, Clin Med Genet, Izmir, Turkey
关键词
Maturity-onset diabetes of the young Type I; macrosomia; HNF4A; monogenic diabetes; child;
D O I
10.4274/jpr.60252
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Maturity-onset diabetes of the young (MODY) is a monogenic form of diabetes, with autosomal-dominant inheritance, which usually develops before 25 years of age. MODY is classically caused by a heterozygous mutation of genes known to affect insulin production or secretion. Heterozygous inactivating hepatocyte nuclear factor 4A (HNF4A) mutations, one of the rare subtypes of MODY, cause impaired insulin secretion and subsequent glucose intolerance especially in adolescence. Conversely, HNF4A mutations are also known to be associated with macrosomia and hyperinsulinemic hypoglycemia in newborns. Herein, we report a rare cause of diabetes resulting from a novel heterozygous mutation in the HNF4A gene. In conclusion, genetic testing should be considered in order to establish an accurate diagnosis and provide an opinion in determining the appropriate type of treatment.
引用
收藏
页码:156 / 160
页数:5
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