一个患有脑的胎儿的复合异构B3GALNT2突变:一个病例报告
Dandan Ling1,2, Wanqin Xie1,3, Xiao Mao1,3
1Clinical Research Center For Placental Medicine In Hunan Province Changsha City China.
Clinical case reports
|April 8, 2024
概括
这项研究确定了B3GALNT2基因中的复合异合体变异为神经管缺陷脑的原因. 这一发现扩大了先天性脑形的已知遗传原因.
科学领域:
- 遗传学 遗传学 是一个
- 发展生物学 发展生物学
- 神经学 神经学
背景情况:
- 脑是一种先天性神经管缺陷,涉及脑组织通过头骨开口突起.
- 遗传因素与神经管缺陷的病因有关,但致病基因尚未完全阐明.
- B3GALNT2 是一种已知的基因,与肌肉缩症有关,这是一组先天性肌肉缩症.
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