由于新型TCF12突变,双边冠状骨同位症的扩展表型
Lingzhao Min1, Jia Wei, Weiwei Mao
1Department of Pediatric Neurosurgery, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Yangpu, Shanghai, China.
The Journal of craniofacial surgery
|June 25, 2025
概括
头骨突,早期的头骨合,可能是由遗传因素引起的. 在患有双边冠状骨突变的患者中发现了一种新的TCF12基因突变,为这种罕见疾病提供了新的见解.
科学领域:
- 遗传学 遗传学 是一个
- 发展生物学 发展生物学
- 儿科医学 儿科医学
背景情况:
- 头骨突症是头骨部的过早融合,影响2200名新生儿中约1名.
- 人们越来越了解非综合征性脑膜异位症的遗传基础,特别是独角形和双角形类型.
- 冠状骨同位症是第二个最常见的形式,仅次于沙吉塔骨同位症.
研究的目的:
- 报告双边冠状骨同位症的病例.
- 在本案中确定该病的遗传原因.
- 描述与这种基因突变相关的新型临床特征.
主要方法:
- 在患者身上进行了整体外基因组测序.
- 基因分析确定了TCF12基因中的特定突变.
- 对父母DNA进行了分离分析.
主要成果:
- 在TCF12基因中发现了一种新的异质合变异 (NM_207037.2;intron16:c.1468-G>T).
- 这种突变是 * de novo * ,在患者的父母中不存在.
- 观察到一种与双边冠状骨同位症相关的新型临床特征.
结论:
- TCF12的一个新型致病变体与双边冠状骨突变有关.
- 这一发现扩大了已知的骨突症的遗传原因.
- 需要进一步的研究,以充分了解TCF12相关的关突突症的遗传和临床谱.
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