[Identification of a Tp63 gene variant in an abortus with Ectrodactyly, Ectodermal dysplasia, Cleft lip/palate syndrome by whole-exome sequencing]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Feb 10;37(2):139-141. doi: 10.3760/cma.j.issn.1003-9406.2020.02.009.
[Article in Chinese]

Abstract

Objective: To detect potential variant in a male fetus suspected for Ectrodactyly, Ectodermal dysplasia, Cleft lip/palate (EEC) syndrome.

Methods: Peripheral blood samples of the fetus and his parents were collected for the extraction of DNA. Whole-exome sequencing was carried out to detect potential variants. Suspected variants were verified by Sanger sequencing.

Results: The fetus was found to carry a heterozygous c.673C>T missense variant of the Tp63 gene, which was known to underlie split-hand/split-foot malformation. The same variant was not found in either parents.

Conclusion: The heterozygous c.673C>T missense variant of the Tp63 gene probably underlies the EEC syndrome in the fetus. Above finding also expanded the phenotypic spectrum for this variant.

Publication types

  • Case Reports

MeSH terms

  • Cleft Lip* / genetics
  • Cleft Palate* / genetics
  • Ectodermal Dysplasia* / genetics
  • Exome Sequencing
  • Humans
  • Limb Deformities, Congenital
  • Male
  • Transcription Factors / genetics*
  • Tumor Suppressor Proteins / genetics*

Substances

  • TP63 protein, human
  • Transcription Factors
  • Tumor Suppressor Proteins

Supplementary concepts

  • Ectrodactyly