单边,双边对称或不对称的隔离性听力损失在患有异合体KITLG变异的患者中
Margaux Serey-Gaut1,2,3, Ralyath Balogoun3, Laurence Jonard3
1Centre de Recherche en Audiologie, Hôpital Necker-Enfants Malades, AP-HP, Paris, France.
Human genetics
|February 7, 2025
概括
证实KITLG基因中的遗传变异会导致孤立的听力损失,包括单边和双边形式. 这一发现支持对早期,非突然听力损失的基因测试.
科学领域:
- 遗传学 是一个遗传学.
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
- 分子生物学分子生物学
背景情况:
- 致病性KITLG变异与听力损失和色素异常有关.
- 需要进一步确认KITLG在孤立性听力损失,特别是单方面听力损失中的作用.
- 基因KITLG是与单边隔离性听力损失相关的主要基因.
研究的目的:
- 确认KITLG在孤立听力损失中的参与.
- 研究基因听力损失患者队列中的KITLG变异.
- 分析与KITLG变异相关的临床表现.
主要方法:
- 对KITLG变异患者的回顾性研究.
- 来自法国遗传性听力损失国家参考网络的队列的分析.
- 通过Genematcher交换平台增加了一个新案例.
主要成果:
- 鉴定了来自八个家族的14名患者的单基KITLG缺失和变异.
- 所有患者都呈现了感觉神经听力损失 (单边,双边对称或不对称).
- 听力损失主要影响低频,而不是深度;不完全的透和轻微的色素变化被注意到.
结论:
- 证实KITLG参与了孤立的单边,双边对称和不对称的听力损失.
- 对KITLG的遗传测试与早期发病,非突然,孤立单边听力损失有关.
- KITLG的改变可能会导致功能丧失,破坏KIT结合.
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