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三例受影响同胞因MED12缺乏导致握拳、手指重叠和马蹄内翻足胎儿的产前诊断:病例报告

Prenatal diagnosis in a fetuses with a clenched hands, overlapping fingers, and clubfoot due to MED12 deficiency in three affected siblings: A case report.

作者信息

Xue Huiqin, Tang Qiaoyin, Feng Yu, Zhao Chenyue, Xu Ke, Gu Weiyue, Xue Zhaoyu, Li Xinyan, Jiang Jinsong, Lu Hongyong, Sun Xiayu, Wu Jianrui, Cao Guizhi

机构信息

Department of Cytogenetic Laboratory, Children's Hospital of Shanxi, Women Health Center of Shanxi, Affiliated Hospital of Shanxi Medical University, Taiyuan, China.

Department of Paediatric Medicine, Shanxi Medical University, Taiyuan, China.

出版信息

Front Genet. 2023 Jul 12;14:1037345. doi: 10.3389/fgene.2023.1037345. eCollection 2023.

Abstract

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.

摘要

胎儿握拳且手指重叠在非整倍体综合征中更为常见,而在MED12缺乏症中记录较少。本研究报告了一个中国家庭中三名患病兄弟姐妹的临床和基因学发现。染色体核型分析图显示,这三个孩子的核型均正常。三联体全外显子组测序和桑格测序验证发现,正常母亲及其两个后代存在MED12 R296Q变异。通过三维超声检查发现,所有三名患病兄弟姐妹均有握拳且手指重叠(手指弯曲)和马蹄内翻足的表现。该病例的发现表明,即使染色体核型正常,当超声检查结果显示有握拳且手指弯曲和马蹄内翻足症状时,仍需要进行全面的产前基因诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7946/10369338/8d59622669d2/fgene-14-1037345-g001.jpg

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