在OTUD5中,一种新的误解变异导致X相关的多种先天性异常-神经发育综合征
Weifang Tian1, Haiyu Li1, Ying Li1
1Prenatal Diagnosis Center, The Third Affiliated Hospital of Zhengzhou University, Maternal and Child Health Hospital of Henan Province, Zhengzhou, China.
Molecular genetics & genomic medicine
|December 1, 2023
概括
这项研究在一个患有X链接多重先天性异常-神经发育综合征 (MCAND) 的中国患者中发现了一种新的OTUD5基因变异,扩大了这种遗传性疾病的已知的临床和分子谱.
科学领域:
- 遗传学 是一个遗传学.
- 神经发育障碍 神经发育障碍
- 罕见疾病是一种罕见的疾病.
背景情况:
- OTUD5基因编码了一种对细胞过程至关重要的二化酶 (DUB).
- OTUD5基因变异与X相关的多种先天性异常 - 神经发育综合征 (MCAND) 有关.
- 了解OTUD5变异是诊断和管理MCAND的关键.
研究的目的:
- 在中国患者中鉴定一种新的OTUD5基因变异.
- 扩大OTUD5相关的MCAND的临床和分子谱.
- 提供已公布的MCAND案件的全面审查.
主要方法:
- 在患者及其父母身上进行了基于三组的临床外体序列测序 (trio-CES).
- 桑格测序用于变种验证.
- 对MCAND案件进行了系统的文献审查.
主要成果:
- 在该患者身上,在OTUD5基因中发现了一种新的误解变异 (c.1305T>A).
- 患者表现出特有的面部特征,智力障碍,全球发育迟缓,四肢收缩和脏异常.
- 这一病例是中国人口中首次报告这种特定的OTUD5变异.
结论:
- 这项研究确定了一种新的OTUD5变异,扩大了MCAND.的遗传场景.
- 与OTUD5变异相关的临床特征显示出显著的表型变异性.
- 这项研究增强了对OTUD5相关的MCAND遗传和临床谱的理解.
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