超血症和同时发生的TBX1突变在糖原储存疾病Ib型:病例报告
Zakaria Kasmi1, Imane Ain El Hayat2, Zahra Aadam3
1Laboratory of Clinical Immunology, Inflammation, and Allergy (LICIA), Faculty of Medicine and Pharmacy of Casablanca, Hassan II University, Casablanca, Morocco. zakariakasmi94@gmail.com.
BMC medical genomics
|January 8, 2025
概括
一个摩洛哥婴儿的糖原储存疾病Ib型 (GSD-Ib) 呈现出异常高血症和TBX1基因变异. 这个案例扩大了对GSD-Ibb的理解.
科学领域:
- 代谢障碍 代谢障碍 代谢障碍
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
背景情况:
- 糖原储存疾病Ib型 (GSD-Ib) 是一种罕见的自体逆性代谢障碍.
- 它是由SLC37A4基因的突变引起的,导致葡萄糖-6-酸盐转位酶缺乏.
- 这种缺乏会损害糖原分解和葡萄糖生成,导致代谢障碍.
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