马兰综合征的可变表达性
1Biochemistry, All India Institute of Medical Sciences, Kalyani, Kalyani, West Bengal, India atanu.biochem@aiimskalyani.edu.in.
BMJ case reports
|October 17, 2024
概括
这项研究确定了一个新的NFIX基因变异在一个家庭的发育延迟和明显的面部特征. 这些发现突出了马兰综合征的可变表达性,影响神经发育在受影响的个体中不同.
科学领域:
- 遗传学 是一个遗传学.
- 神经发育障碍 神经发育障碍
- 临床医学 临床医学
背景情况:
- 马兰综合征是一种罕见的遗传性疾病,其特点是发育迟缓,智力障碍和独特的面部特征.
- NFIX基因在大脑发育中起着至关重要的作用,NFIX基因的突变与各种神经发育状况有关.
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