| Literature DB >> 28371085 |
Nicola Dikow1, Martin Granzow1, Luitgard M Graul-Neumann2, Stephanie Karch3, Katrin Hinderhofer1, Nagarajan Paramasivam4,5, Laura-Jane Behl6, Lilian Kaufmann1, Christine Fischer1, Christina Evers1, Matthias Schlesner5, Roland Eils5,7, Guntram Borck8, Christiane Zweier9, Claus R Bartram1, John C Carey10, Ute Moog1.
Abstract
Recently, de novo heterozygous variants in DDX3X have been reported in about 1.5% of 2659 females with previously unexplained intellectual disability (ID). We report on the identification of DDX3X variants in two unrelated girls with clinical features of Toriello-Carey Syndrome (T-CS). In patient 1, the recurrent variant c.1703C>T; p.(P568L) was identified when reconsidering X-linked de novo heterozygous variants in exome sequencing data. In patient 2, the DDX3X variant c.1600C>G; p.(R534G) was also detected by exome sequencing. Based on these data, de novo heterozygous DDX3X variants should be considered not only in females with unexplained ID, but also in individuals with a clinical diagnosis of T-CS.Entities:
Keywords: DDX3X; Toriello-Carey syndrome; exome sequencing; intellectual disability
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Year: 2017 PMID: 28371085 DOI: 10.1002/ajmg.a.38164
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802