Genetic testing of 10 patients with features of Loeys-Dietz syndrome

Clin Chim Acta. 2016 May 1:456:144-148. doi: 10.1016/j.cca.2016.02.005. Epub 2016 Feb 11.

Abstract

Inherited aortopathy, characterized with a high risk of fetal aortic aneurysms/dissections, could occur secondary to several syndromes. To identify genetic mutations and help to give a precise diagnosis, we performed a gene panel testing, involving 15 genes related to inherited aortopathy. Here we reported 10 patients, combining with the genetic testing results, were diagnosed or suspected with Loeys-Dietz syndrome, which would be the largest group of Loeys-Dietz syndrome ever reported in China till now. 10 likely pathogenic mutations or rare variants of uncertain significance were found. These results expanded the mutation spectrum of Loeys-Dietz syndrome and might be implicated in its wide phenotypic spectrum.

Keywords: Genetic testing; Loeys Dietz syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aortic Aneurysm / complications
  • Child
  • Child, Preschool
  • Female
  • Genetic Testing*
  • Humans
  • Loeys-Dietz Syndrome / complications
  • Loeys-Dietz Syndrome / diagnosis*
  • Loeys-Dietz Syndrome / genetics*
  • Male
  • Middle Aged
  • Mutation