患有LHX3基因病原性拼接变异的患者的听力损伤和前庭功能
Åsa Kjellgren1, Elenor Lundgren1, Irina Golovleva2
1Department of Clinical Sciences, Otorhinolaryngology, University of Umeå, Umeå, Sweden.
BMC medical genomics
|November 16, 2024
概括
一种特定的LHX3基因变异导致渐进性听力损失和前庭功能障碍. 这种创始突变突出了LHX3基因在耳和平衡器官功能中的关键作用.
科学领域:
- 遗传学 遗传学 是一个
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
- 神经科学是一个神经科学.
背景情况:
- LHX3基因编码了一个LIM - 宿主体转录因子,对胎儿发育至关重要,包括垂体腺,脊柱运动神经元和内耳.
- 在LHX3的致病变体是罕见的,并导致结合性垂体激素缺陷-3 (CPHD3).
研究的目的:
- 为了研究具有特定LHX3基因变异的个体的听力和前庭功能.
- 确定LHX3基因在听觉和前庭系统发育和功能中的作用.
主要方法:
- 研究了8个 (8-36岁) 个体,对LHX3基因变异具有同胞性.
- 分析了从出生到2024年4月连续的听力测试.
- 对6名患者进行了前庭检测.
主要成果:
- 所有患者都表现出渐进的感觉神经听力损失,从中度到完全.
- 在6名患者中,静脉检测显示出与此相关的静脉功能障碍.
- 这是首次证明LHX3基因突变会影响前庭功能.
结论:
- 在LHX3中,人类致病变体c.455-2A>G是导致渐进性听力损失和平衡障碍的原因.
- 这种变异在瑞典北部人口中充当创始基因突变.
- LHX3基因对于耳和前置器官的正常功能至关重要.
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