案例报告:整体外基因组测序在儿童发育迟缓的TRAPPC9基因中识别了复合异合体变异体
Bingxuan Yu1,2, Jing Chen1,2, Shuo Yang1,2
1Department of Medical Genetics/Prenatal Diagnostic Center, West China Second University Hospital, Sichuan University, Chengdu, China.
Frontiers in genetics
|August 26, 2024
概括
在TRAPPC9基因中发现的复合异合体变异被认为是导致一个年轻的中国女孩的全球发育迟缓的原因. 这一发现强调了基因检测发育障碍和产前诊断的重要性.
科学领域:
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
- 分子生物学分子生物学
背景情况:
- 全球发育迟缓影响全球5岁以下儿童的10-15%.
- 多种因素导致发育迟缓,包括遗传倾向.
- 特定的基因变异,如EFNB1,MECP2和TRAPPC9中的变异,都与发育障碍有关.
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