Identification of a novel gene variant in a patient with an intellectual development disorder: a literature review and case report.

belongs to a family of protein lysine methyltransferases that methylate non-histone proteins. Recently, the gene has been reported to be related to an intellectual developmental disorder, autosomal recessive 44. Patients present with developmental delay, intellectual disability (ID), and variable dysmorphic features. Here, we report on a Chinese girl who presented with global developmental delay, abnormal brain structure, and multiple facial deformities, including a short/upturned nose with a sunken bridge, thin lips, and flat occiput. Whole-exome sequencing identified a novel variant (NM_001080510.5: c.322+1del) on the gene. This variant was not collected on public human variants databases such as gnomAD, predicted to influence the splicing as a classical splicing variant, and classified as Pathogenic according to the American College of Medical Genetics and Genomics (ACMG) guidelines. Since patients with -related ID are rare, we summarize and compare the clinical phenotype of reported patients with variants. Our report further expands the variants and provides new evidence for clinical diagnosis of -related ID.