与GREB1L相关的人类疾病的扩大范围可能包括复杂的先天性心脏病
Emily Zhao1, Miles Bomback2, Atlas Khan3
1Department of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Prenatal diagnosis
|January 29, 2024
概括
GREB1L的遗传变异与一系列先天性异常有关,包括脏,心脏和听力问题. 建议对先天性心脏病和相反进行GREB1L测试.
科学领域:
- 遗传学 是一个遗传学.
- 发展生物学 发展生物学
- 临床医学 临床医学
背景情况:
- GREB1L基因变异与波特序列等产前疾病有关.
- 目前尚不完全了解GREB1L相关表型的全部范围.
- 了解GREB1L的作用对于诊断和管理先天性异常至关重要.
研究的目的:
- 综合描述GREB1L.的产前和产后表型谱.
- 为了识别与GREB1L基因变异相关的新型表型.
- 为了让临床医生更好地了解GREB1L相关疾病.
主要方法:
- 通过胎儿测序联盟确定病例.胎儿测序联盟.
- 基于人口的基因组数据库的选.
- 广泛的文献审查以确定GREB1L相关疾病病例.
主要成果:
- 确定了127个具有51个独特的致病性GREB1L变异的个体.
- 脏异常是最常见的 (47%),其次是多个系统异常 (37%),包括低可塑性左心综合征.
- 其他发现包括感觉神经听力损失 (10%) 和子宫发育 (4%).
结论:
- GREB1L变种可以导致人类复杂的先天性心脏病.
- 考虑对患有先天性心脏病的患者进行GREB1L基因测试.
- 建议对具有已识别的GREB1L变异的个人进行心脏查.
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