Frontiers in Genetics (Jul 2023)

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

  • 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

DOI
https://doi.org/10.3389/fgene.2023.1037345
Journal volume & issue
Vol. 14

Abstract

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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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