| Literature DB >> 29753921 |
Wei Shen1, Patti Krautscheid2, Audrey M Rutz3, Pinar Bayrak-Toydemir4, Sarah L Dugan3.
Abstract
De novo variants of ASH1L, which encodes a histone methyltransferase, have been reported in a few patients with intellectual disability and autistic features. Here, we identified a novel de novo frame-shift variant, c.2422_2423delAAinsT which predicts p.(Lys808TyrfsTer40), in ASH1L in a patient with multiple congenital anomalies (MCA), fine motor developmental delay, learning difficulties, attention deficit hyperactivity disorder, sleep apnea, and scoliosis. This frame-shift variant is expected to result in loss-of-function. Our report provides further evidence to support loss-of-function alterations of ASH1L as causative for an emergent neurodevelopmental syndrome characterized by MCA, intellectual disability, and behavioral problems, and further delineates this genetic disorder.Entities:
Keywords: Autism spectrum disorder; Exome sequencing; Intellectual disability; Multiple congenital anomalies
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Year: 2018 PMID: 29753921 DOI: 10.1016/j.ejmg.2018.05.003
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708