埃及婴儿的多诺休综合征:一个病例报告
Kotb Abbass Metwalley1, Hekma Saad Farghaly1, Lamiaa Mahmood Maxi1
1Department of Pediatrics, Faculty of Medicine, Assiut University, Assiut, Egypt.
Case reports in perinatal medicine
|March 5, 2025
概括
多诺休综合征 (DS) 是一种罕见的遗传疾病,导致婴儿严重抗胰岛素. 这个案例突出了典型的特征和高剂量胰岛素的成功血糖控制.
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:
- 多诺休综合征 (DS) 是一种极其罕见的,自体相衰退性遗传疾病.
- 它的特点是严重的胰岛素耐药性和从出生开始的相关代谢并发症.
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