斜向
核型
外显子组测序
马蹄内翻足
桑格测序
外显子组
医学
产前诊断
遗传学
染色体
生物
怀孕
胎儿
DNA测序
表型
基因
畸形
作者
Huiqin Xue,Qiaoyin Tang,Yu Feng,Chenyue Zhao,Ke Xu,Weiyue Gu,Zhaoyu Xue,Xinyan Li,Jinsong Jiang,Hongyong Lu,Xiayu Sun,Jianrui Wu,Guizhi Cao
标识
DOI:10.3389/fgene.2023.1037345
摘要
A fetal clenched hand with overlapping fingers is more common in aneuploidy syndrome and was not well-documented in MED12 deficiency. This study reports the clinical and genetic findings of three affected siblings from a Chinese family. The chromosome karyotype analysis diagram shows that karyotypes of the three children were normal. Trio whole-exome sequencing and Sanger sequencing verification found that there was a MED12 R296Q variant in normal mothers and their two offspring. A pattern of clenched hand with overlapping fingers (clinodactyly) and clubfoot was found in all the three affected siblings by three-dimensional ultrasound. The discovery of this case shows that even if the chromosome karyotype is normal, comprehensive prenatal genetic diagnosis is required when the ultrasound results show a clenched hand with clinodactyly and clubfoot symptoms.
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