Affiliation:
1. Department of Clinical and Experimental Sciences University of Brescia Brescia Italy
2. Unit of Child Neurology and Psychiatry ASST‐Spedali Civili of Brescia Brescia Italy
Abstract
AbstractPUS7 gene pathogenic variants cause a deficiency in an RNA‐independent pseudouridine synthase, which results in a neurodevelopmental phenotype characterized by various degrees of psychomotor delay, acquired microcephaly, aggressive behavior, and intellectual disability. Since 2018, PUS7 deficiency has been described in 15 patients with different pathogenic variants but similar clinical phenotypes. We describe the case of a male infant with a homozygous truncating pathogenic variant in the PUS7 gene (c.329_332delCTGA; p.Thr110Argfs*4) who, in addition to the previously mentioned features, displays self‐injurious behavior, sleep disturbances and motor stereotypies.
Subject
Genetics (clinical),Genetics