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Updated: Jul 12, 2025

Hyperinsulinemic-euglycemic Clamps in Conscious, Unrestrained Mice
Published on: November 16, 2011
一个患有KMT2D-关联卡布基综合征的患者的持续性低血糖和高胰岛素症
Mariana Nunez Stosic1, Patricia Gomez1
1Pediatric Endocrinology, University of Miami, Miami, FL 33136, USA.
这项案例研究突出了由于KMT2D基因突变导致的卡布基综合征 (KS) 的儿童持续性高胰岛素血糖低血症. 早期诊断和管理对于这种罕见但严重的KS并发症至关重要.
科学领域:
- 遗传学 是一个遗传学.
- 内分泌学 在内分泌学.
- 儿科 儿科 儿科
背景情况:
- 卡布基综合征 (KS) 是一种罕见的遗传性疾病,其特征是发育迟缓,面部特征变形和器官形.
- 超胰岛素性低血糖是已知的,虽然不常见的KS并发症,特别是KS2型 (KDM6A).
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