在46XY性别发展差异的兄弟姐妹中,与LARS2相关的佩罗氏综合征
Aaron P Adam1, Lauren O'Sullivan2, Amanda Peterson2
1Department of Biology, Stanford University, Stanford, California, USA.
American journal of medical genetics. Part A
|March 22, 2025
概括
与LARS2相关的男性佩罗氏综合征的特征是听力损失和低维力化,包括未下降的丸和低度. 本案例报告强调了在XY个体中考虑LARS2基因变异的重要性,这些人有性发育障碍和听力损失.
科学领域:
- 遗传学 是一个遗传学.
- 内分泌学 在内分泌学.
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
背景情况:
- 佩罗综合征在XX个体中表现为感觉神经听力损失和卵巢功能障碍.
- 很少报告XY个体患有佩罗综合征的低 virilization.
- LARS2基因与生殖腺发育和生育有关.
研究的目的:
- 报告两名兄弟患有与LARS2相关的佩罗氏综合征,表现出低病毒化.
- 为了强调LARS2变异在XY个体与佩罗综合征的意义.
- 建议LARS2用于46,XY个体的差异诊断,患有DSD和听力损失.
主要方法:
- 两个受影响的兄弟的案例报告.
- 四重外体序列测定用于识别遗传变异.
- 听力损失和病毒化状态的临床评估.
主要成果:
- 两兄弟都出现了双边深度感官神经神经听力损失.
- 两个兄弟都有双边未下降的丸,需要手术干预.
- 小弟弟也患有带带的低;在LARS2中确定了双基致病变体.
结论:
- 低 virilization 是一个未被认可的特征 LARS2 相关的佩罗氏综合征在46,XY个体.
- 在对46,XY个体的差异诊断中应考虑LARS2 DSD和听力损失.
- 这扩大了LARS2相关的Perrault综合征已知的表型.
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