在CONT3中发现的新突变导致IDDSADF:一个病例报告和文献综述
Mengxiong Pan1,2, Hui Li3, Liming Pan3
1Department of Neurology, The First People's Hospital of Huzhou, Huzhou, China.
The Journal of international medical research
|August 31, 2024
概括
在一个中国患者身上发现了一种新的CONT3基因突变,该患者患有智力发育障碍,言语迟缓,自闭症和异形面部 (IDDSADF). 这一发现扩大了IDDSADF相关疾病的已知CONT3突变特征.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
- 发展生物学 发展生物学
背景情况:
- CONT3基因对mRNA转录和蛋白质翻译至关重要.
- 在CONT3突变与智力发育障碍与言语延迟,自闭症和异形面部 (IDDSADF) 相关.
- 在IDDSADF中报告了很少的CONT3突变.
研究的目的:
- 在患有IDDSADF的患者中报告一种新的CONT3突变.
- 在IDDSADF中扩大CONT3已知的突变谱.
- 为了为IDDSADF的基因特异性诊断提供基础.
主要方法:
- 整个外体组的测序.
- 直接的桑格尔测序 直接的桑格尔测序
- 临床病例报告报告
主要成果:
- 在一名中国患者身上发现了CONT3的第14个外基因c.1616_1623del突变.
- 患者呈现出发育迟缓,言语回归和面部形.
- 大脑MRI显示侧心室扩张.
结论:
- 这是CONT3.的c.1616_1623del位点发生病原性突变的第一次报告.
- 鉴定到的突变扩大了CONT3对IDDSADF的突变概况.
- 这种情况有助于对IDDSADF相关疾病的基因特异性诊断.
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