A novel variant in the QRICH1 gene was identified in a patient with severe developmental delay

Abstract

AbstractBackgroundQRICH1 encodes the glutamine‐rich protein 1, which contains one caspase activation recruitment domain and is likely to be involved in apoptosis and inflammation. However, the function of the QRICH1 gene was largely unknown. Recently, several studies have reported de novo variants in QRICH1, and the variants have been associated with Ververi‐Brady syndrome characterized by developmental delay, nonspecific facial dysmorphism, and hypotonia.Materials and MethodsWhole exome sequencing, clinical examinations, and functional experiments were performed to identify the etiology of our patient.ResultsHere, we added another patient with severe growth retardation, atrial septal defect, and slurred speech. Whole exome sequencing identified a novel truncation variant in the QRICH1 gene (MN_017730.3: c.1788dupC, p.Tyr597Leufs*9). Furthermore, the functional experiments confirmed the effect of genetic variation.ConclusionOur findings expand the QRICH1 variant spectrum in developmental disorders and provide evidence for the application of whole exome sequencing in Ververi‐Brady syndrome.