两个姐妹的故事 - 遗传性高胰岛素性低血糖症的延迟诊断
F Stringer1, C Preston1,2, R MacIsaac1,3
1Departments of Endocrinology and Diabetes, Surgery and General Medicine, St Vincent's Hospital Melbourne and the University of Melbourne, Victoria, Australia.
Endocrinology, diabetes & metabolism case reports
|August 17, 2024
概括
先天性高胰岛素症是一种罕见的疾病,可以在成年时被诊断出来. 两位患有ABCC8基因变异的成年姐妹被诊断出患有高胰岛素性低血糖症,这凸显了成人病例需要提高认识的必要性.
科学领域:
- 内分泌学 在内分泌学.
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
背景情况:
- 先天性高胰岛素症 (CHI) 是儿童持续低血糖的主要原因.
- 成年人诊断CHI是不常见的,但有可能.
- 肝炎呈现类似于胰岛素瘤,需要仔细区分.
研究的目的:
- 报告两位成年姐妹被诊断患有先天性高胰岛素症.
- 要突出晚发性CHI的遗传基础 (ABCC8基因变体).
- 讨论成人CHI的诊断和管理策略.
主要方法:
- 两位成年姐妹的案例报告.
- 基因分析识别了ABCC8基因中化合物异构合的可能致病变体.
- 对临床表现,研究和治疗的审查.
主要成果:
- 两位姐妹在47岁和57岁被诊断出患有高胰岛素性低血糖症.
- 诊断证实了ABCC8基因中复合异构合的可能致病变体.
- 讨论典型的特征,调查和治疗.
结论:
- 先天性高胰岛素症可以在成年时出现,通常是由于ABCC8或KCNJ11基因变异.
- 治疗可能涉及对医疗无反应的患者的二氧化或持续的葡萄糖监测.
- 提高认识对于及时诊断和管理成人发作的CHI至关重要.
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