儿童患者与先天性腹相关的DGAT1突变:一个病例报告
Asim Mehmood1, Rida Inam1, Nimra Rabbani1
1Internal Medicine, Shifa College of Medicine, Islamabad, PAK.
Cureus
|August 22, 2024
概括
基因测试确定了二甲基甘酸转移酶1 (DGAT1) 缺乏作为婴儿慢性腹的原因. 早期诊断和营养支持导致了临床改善,突出显示了遗传分析在先天性肠道病变中的重要性.
科学领域:
- 儿科胃肠病学 儿科胃肠病学
- 临床遗传学 临床遗传学
- 分子医学是分子医学.
背景情况:
- 婴儿慢性腹带来了诊断上的挑战,往往需要超越常见病因的调查.
- 先天性肠病,即从出生就存在的肠功能障碍,可以表现为持续的胃肠道症状.
- 糖醇转移酶1 (DGAT1) 缺乏症是一种罕见的遗传疾病,影响脂质代谢和肠道功能.
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