| Literature DB >> 35707592 |
Naoto Nishimura1,2, Yumi Enomoto3, Tatsuro Kumaki1, Hiroaki Murakami1, Azusa Ikeda4, Tomohide Goto4, Kenji Kurosawa1.
Abstract
Say-Barber-Biesecker-Young-Simpson syndrome (SBBYSS) and genitopatellar syndrome (GPS) are caused by variants of lysine acetyltransferase 6B (KAT6B). These variants tend to occur in the terminal exons of KAT6B. Here, we report a patient with global developmental delay, intellectual disability, autistic behavior, muscular hypotonia, facial dysmorphism, and seizures caused by a novel missense variant in exon 7 of KAT6B. The patient showed a phenotype differing from those of SBBYSS and GPS. We also report patients with missense variants in the proximal exons of KAT6B showing dysmorphic features and autistic behavior not resembling the characteristics of SBBYSS and GPS. Missense variants in the proximal exons of KAT6B may have a dominant negative effect or cause gain of function, leading to unique phenotypes not resembling those of SBBYSS and GPS.Entities:
Keywords: Genitopatellar syndrome; Genotype-phenotype correlation; Lysine acetyltransferase 6B; Say-Barber-Biesecker-Young-Simpson syndrome; Whole-exome sequencing
Year: 2022 PMID: 35707592 PMCID: PMC9149453 DOI: 10.1159/000520134
Source DB: PubMed Journal: Mol Syndromol ISSN: 1661-8769