ABSTRACT
Diagnostic exome sequencing (DES) has aided delineation of the phenotypic spectrum of rare genetic etiologies of intellectual disability (ID). A SET domain containing 5 gene (SETD5) phenotype of ID and dysmorphic features has been previously described in relation to patients with 3p25.3 deletions and in a few individuals with de novo sequence alterations. Herein, we present additional patients with pathogenic SETD5 sequence alterations. The majority of patients in this cohort and previously reported have developmental delay, behavioral/psychiatric issues, and variable hand and skeletal abnormalities. We also present an apparently unaffected carrier mother of an affected individual and a carrier mother with normal intelligence and affected twin sons. We suggest that the phenotype of SETD5 is more complex and variable than previously presented. Therefore, many features and presentations need to be considered when evaluating a patient for SETD5 alterations through DES.
Subject(s)
Body Dysmorphic Disorders/genetics , Developmental Disabilities/genetics , Intellectual Disability/genetics , Methyltransferases/genetics , Adolescent , Adult , Body Dysmorphic Disorders/diagnosis , Body Dysmorphic Disorders/physiopathology , Child , Child, Preschool , Chromosome Deletion , Chromosomes, Human, Pair 3/genetics , Developmental Disabilities/diagnosis , Developmental Disabilities/physiopathology , Female , Humans , Infant , Intellectual Disability/diagnosis , Intellectual Disability/physiopathology , Male , Middle Aged , Mutation/genetics , Penetrance , Phenotype , Exome Sequencing , Young AdultABSTRACT
Graphical abstract key: ADHD, attention deficit hyperactivity disorder; ASD, atrial septal defect; DD, developmental delay; EEG, electroencephalogram; Ht, height; ID, intellectual disability; OCD, obsessive-compulsive disorder; OFC, open fontanelle; PDA, patent ductus arteriosis; PFO, patent foramen ovale; VSD, ventricular septal defect; Wt, weight.