| Literature DB >> 29928181 |
Sara Vanegas1, Diana Ramirez-Montaño1, Estephania Candelo1, Marwan Shinawi2, Harry Pachajoa1,3.
Abstract
Pathogenic variants in WAC are uncommon causes of developmental delay and neurobehavioral phenotypes. The clinical features associated with WAC haploinsufficiency include recognizable dysmorphic facial features that were recently delineated as DeSanto-Shinawi syndrome (DESSH; OMIM 616708). Additional clinical features include hypotonia, hearing and vision abnormalities, gastrointestinal problems, and behavioral difficulties. Here, we report a case of a 4-year-old Colombian male patient with typical dysmorphic facial features, developmental delay, hyperactivity, and recurrent respiratory infections. His immune workup revealed hypogammaglobulinemia, and clinical exome sequencing revealed a novel intronic variant in WAC (c.1437+1G>A). To the best of our knowledge, this is the first case of DESSH in South America, underlining the accumulating evidence of the significant role of WAC haploinsufficiency in neurobehavioral phenotypes. Although this report suggested the potential involvement of WAC in immune regulation, additional reports are required to confirm our observations.Entities:
Keywords: Dysmorphic facial features; Intellectual disability; WAC
Year: 2018 PMID: 29928181 PMCID: PMC6006642 DOI: 10.1159/000488815
Source DB: PubMed Journal: Mol Syndromol ISSN: 1661-8769