在患有脏异常的胎儿中,一种新的NONO无意义变异
Laia Rodriguez-Revenga1,2, Alfons Nadal3,4, Virginia Borobio5
1Biochemistry and Molecular Genetics Department, Hospital Clinic of Barcelona and Fundacio de Recerca Clínic Barcelona-Institut d'Investigacions Biomediques August Pi i Sunyer (FRCB-IDIBAPS), Barcelona, Spain.
在一个胎儿中发现了一种新的NONO基因变异,胎儿患有多种异常,包括脏缺陷. 这一发现扩大了已知的X链接智力发育障碍的产前表型,综合征34.
科学领域:
- 遗传学 遗传学 是一个
- 医学遗传学 医学遗传学
- 发展生物学 发展生物学
背景情况:
- 智力发育障碍,X链接综合征34 (OMIM#300967) 是一种罕见的疾病.
- 这种疾病的产前表型尚不清楚,大多数病例呈现出先天性心脏缺陷.
研究的目的:
- 报告一种新的致病性NONO变种.
- 描述与这种变体相关的产前表型,包括以前未报告的脏异常.
主要方法:
- 胎儿超声波在16 + 6周怀孕.
- 三元外基因组测序. 三元外基因组测序.
- 尸检后的检查. 尸检后的检查.
主要成果:
- 在NONO基因中检测到一种新的 de novo 半性致病性功能丧失变异.
- 产前超声检查显示,右多囊性形性脏,左性瘤发生,尿膀缺失,心肌缩,部折叠增加,单动脉,以及小水.
- 尸体解剖证实了超声波的发现,并确定了肺部低成形症,逆鼻症和低置耳朵.
结论:
- 这个案例突出显示了智力发育障碍的产前谱中的新异常,X链接综合征34.
- 需要进一步临床划分才能充分描述与NONO变体相关的产前表型.
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