病例报告:由于AKT2中的激活变体而导致的低胰岛素性低性低血糖症
Laura Sayol-Torres1, Ariadna Campos-Martorell1, Julia Sala-Coromina2
1Department of Paediatric Endocrinology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Journal of clinical research in pediatric endocrinology
|August 11, 2025
概括
一种罕见的AKT2基因突变会导致严重的低血糖和发作. 持续的葡萄糖监测有助于诊断和管理,显示缩短的禁食时间改善了结果.
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:
- AKT2基因对于胰岛素信号传递至关重要.
- 在AKT2中获得功能突变 (c.49G>A,p.Glu17Lys) 与严重的低血糖症,半高缩和肥胖症有关.
- 在AKT2变异的患者中存在表型变异.
研究的目的:
- 报告一个AKT2功能增益突变的新案例.
- 突出持续血糖监测 (CGM) 在诊断和管理中的有用性.
- 讨论表型谱和管理策略.
主要方法:
- 整体外因子测序确定了AKT2变种.
- 持续血糖监测 (CGM) 用于诊断和监测.
- 分析了临床数据和患者病史.
主要成果:
- 一名12岁的男孩出现了发作,形状不佳的特征和智力障碍.
- 遗传分析显示,AKT2中存在一个异合的误解变体 (c.49G>A,p.Glu17Lys).
- CGM检测到严重的低血糖,早晨占主导地位,与发作相吻合;减少禁食的管理改善了结果.
结论:
- 这种情况扩大了已知的AKT2功能增益突变的表型,包括对称过度生长.
- 持续的葡萄糖监测是诊断和管理AKT2相关低血糖症的宝贵工具.
- 早期诊断和量身定制的管理,包括缩短禁食时间,对于改善患者的治疗结果至关重要.
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