[与TUBB基因c.155A>G变异相关的大脑结构异常的遗传分析和产前诊断]
Yifan Liu1, Wei Song, Xinlian Wang
1Prenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing 100026, China. yys_521@ccmu.edu.cn.
概括
一个中国家庭.
科学领域:
- 遗传学 遗传学 是一个
- 神经科学是一个神经科学.
- 医学诊断 医学诊断 医学诊断
背景情况:
- 结构性脑部异常可能源于遗传突变.
- TUBB基因在神经元发育中起着至关重要的作用.
- 了解基因型-表型相关性对于遗传咨询至关重要.
研究的目的:
- 为了研究一个中国家庭中结构性脑部异常的遗传基础.
- 为了探索TUBB基因变异的基因型-表型相关性.
- 为患有类似疾病的家庭提供产前诊断服务.
主要方法:
- 在怀疑胎儿大脑异常的家庭中进行了产前诊断.
- 使用了染色体副本数变异测序 (CNV-seq) 和三元整体外基因组测序 (Trio-WES).
- 候选变体通过桑格测序得到证实.
主要成果:
- 产前成像显示了中线偏差,腹腔大和旋转不对称.
- 在T.U.B.B.基因 (c.155A>G,p.N52S) 中,Trio-WES发现了一种母性遗传的异质合体误解变异.
- 这种变异被归类为可能致病性,并与受影响个体的类似神经影像发现有关.
结论:
- 鉴定到的TUBB基因变异 (c.155A>G,p.N52S) 很可能是观察到的大脑结构异常的原因.
- 这一发现扩大了这种TUBB变异的已知表型谱.
- 这项研究有助于产前诊断和对受影响家庭的遗传咨询.
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