Article
Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia.
Journal of diabetes investigation - 1 Jan 2024
Wang Yanfei, Xiao Xiaoyu, Lin Qiuqiu, Song Rong, Wang Xiaozhou, Liang Yiji, Chen Jingsong, Luan Xiaojun, Zhou Zhiguang, Xiao Yang, Xue Yaoming, Hu Jingyi
Abstract excerpt
AIMS: HNF1B syndrome is caused by defects in the hepatocyte nuclear factor 1B (HNF1B) gene, which leads to maturity-onset diabetes of the young type 5 and congenital organ malformations. This study aimed to identify a gene defect in a patient presenting with diabetes and severe diarrhea, while also analyzing the prevalence of hypomagnesemia and its correlation with the HNF1B genotype. MATERIALS AND METHODS: Whole...
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