| Literature DB >> 31643139 |
Pauline Marzin1, Sophie Rondeau1, Kimberly A Aldinger2, Jean-Luc Alessandri3, Bertrand Isidor4, Delphine Heron5, Boris Keren5, William B Dobyns2,6, Valérie Cormier-Daire1.
Abstract
The common genes responsible for overgrowth syndromes play key roles in regulating transcription through histone modification and chromatin modeling. The SETD2 gene encoding a H3K36 trimethyltransferase is implicated in Sotos-like syndrome. This syndrome is characterized by postnatal overgrowth, macrocephaly, obesity, speech delay, and advanced carpal ossification. We report four new patients with constitutional SETD2 mutations and review nine earlier reported patients. Almost all patients presented with macrocephaly associated with advanced stature and obesity in half of the cases. In addition to these principal manifestations, neurodevelopmental disorders are common such as intellectual disability (83%), autism spectrum disorders (89%), and behavioral difficulties (100%) with aggressive outbursts (83%). A variety of features such as joint hypermobility (29%), hirsutism (33%), and naevi (50%) were also reported. Constitutional SETD2 mutations are intragenic loss-of-function variants with truncating (69%) and missense (31%) mutations. Functional studies are necessary to improve understanding of the pathogenicity of some missense SETD2 mutations.Entities:
Keywords: SETD2; autism spectrum disorder; histone methyltransferases; overgrowth
Mesh:
Substances:
Year: 2019 PMID: 31643139 DOI: 10.1002/ajmg.c.31746
Source DB: PubMed Journal: Am J Med Genet C Semin Med Genet ISSN: 1552-4868 Impact factor: 3.908