[Analysis of MYH3 gene variation and prenatal diagnosis for two pedigrees affected with congenital arthrogryposis]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 May 10;36(5):447-450. doi: 10.3760/cma.j.issn.1003-9406.2019.05.008.
[Article in Chinese]

Abstract

Objective: To explore the genetic etiology of two pedigrees affected with congenital arthrogryposis.

Methods: Whole exome sequencing (WES) was used to screen potential variations in the proband. Suspected variations were analyzed with bioinformatics software and validated by Sanger sequencing.

Results: A heterozygous c.1123G>A (p.Glu375Lys) variation was detected in the proband and an affected fetus from pedigree 1, while a de novo heterozygous c.118 G>A (p.Val40Met) variation was detected in an affected fetus from pedigree 2.

Conclusion: The two heterozygous variations of the MYH3 gene probably underlie the disease in the pedigrees. Above results have facilitated genetic counseling and prenatal diagnosis.

MeSH terms

  • Arthrogryposis*
  • Cytoskeletal Proteins / genetics*
  • Exome Sequencing
  • Female
  • Heterozygote
  • Humans
  • Mutation
  • Pedigree
  • Pregnancy
  • Prenatal Diagnosis

Substances

  • Cytoskeletal Proteins
  • MYH3 polypeptide, human