| Literature DB >> 26877057 |
Mingyao Luo1, Hang Yang2, Kunlun Yin2, Qianlong Chen2, Jing Zhang1, Yuxin Fan3, Zhou Zhou4, Qian Chang5.
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.Entities:
Keywords: Genetic testing; Loeys Dietz syndrome
Mesh:
Year: 2016 PMID: 26877057 DOI: 10.1016/j.cca.2016.02.005
Source DB: PubMed Journal: Clin Chim Acta ISSN: 0009-8981 Impact factor: 3.786