案例报告:凝血因子XI的等位基和双等位基变异导致XI因子缺乏
Chen Liang1,2, Jie-Yuan Jin3, Hai-Hong Shi2
1Department of Clinical Research, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Frontiers in cardiovascular medicine
|November 28, 2024
概括
十一因子缺乏症是一种罕见的遗传性出血障碍,是由F11基因的变异引起的. 这项研究确定了一种新的F11变种,扩大了基因诊断的知识.
科学领域:
- 血液学 血液学 血液学
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
背景情况:
- 十一因子缺乏症是一种罕见的遗传性凝血障碍,大约影响100万分之一的人.
- 它呈现出轻微的,可变的出血症状,如伤,鼻血和产后出血.
- 这种疾病是由凝血因子XI (F11) 基因的变异引起的.
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