{Reference Type}: Journal Article
{Title}: Expansion of the Genotypic and Phenotypic Spectrum of ASH1L-Related Syndromic Neurodevelopmental Disorder.
{Author}: Cordova I;Blesson A;Savatt JM;Sveden A;Mahida S;Hazlett H;Rooney Riggs E;Chopra M; ;
{Journal}: Genes (Basel)
{Volume}: 15
{Issue}: 4
{Year}: 2024 03 28
{Factor}: 4.141
{DOI}: 10.3390/genes15040423
{Abstract}: Pathogenic ASH1L variants have been reported in probands with broad phenotypic presentations, including intellectual disability, autism spectrum disorder, attention deficit hyperactivity disorder, seizures, congenital anomalies, and other skeletal, muscular, and sleep differences. Here, we review previously published individuals with pathogenic ASH1L variants and report three further probands with novel ASH1L variants and previously unreported phenotypic features, including mixed receptive language disorder and gait disturbances. These novel data from the Brain Gene Registry, an accessible repository of clinically derived genotypic and phenotypic data, have allowed for the expansion of the phenotypic and genotypic spectrum of this condition.