Literature DB >> 35707592

Delineation of a Phenotype Caused by a KAT6B Missense Variant Not Resembling Say-Barber-Biesecker-Young-Simpson and Genitopatellar Syndromes.

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.
Copyright © 2022 by S. Karger AG, Basel.

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


  3 in total

1.  A female patient with X-linked Ohdo syndrome of the Maat-Kievit-Brunner phenotype caused by a novel variant of MED12.

Authors:  Hiroaki Murakami; Yumi Enomoto; Yoshinori Tsurusaki; Yoshitsugu Sugio; Kenji Kurosawa
Journal:  Congenit Anom (Kyoto)       Date:  2019-07-29       Impact factor: 1.409

2.  A novel truncating variant within exon 7 of KAT6B associated with features of both Say-Barber-Bieseker-Young-Simpson syndrome and genitopatellar syndrome: Further evidence of a continuum in the clinical spectrum of KAT6B-related disorders.

Authors:  Giuseppe Marangi; Marilena C Di Giacomo; Serena Lattante; Daniela Orteschi; Sara Patrizi; Paolo N Doronzio; Francesco N Riviello; Alessandro Vaisfeld; Silvia Frangella; Marcella Zollino
Journal:  Am J Med Genet A       Date:  2017-12-11       Impact factor: 2.802

3.  CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions.

Authors:  Darci T Butcher; Cheryl Cytrynbaum; Andrei L Turinsky; Michelle T Siu; Michal Inbar-Feigenberg; Roberto Mendoza-Londono; David Chitayat; Susan Walker; Jerry Machado; Oana Caluseriu; Lucie Dupuis; Daria Grafodatskaya; William Reardon; Brigitte Gilbert-Dussardier; Alain Verloes; Frederic Bilan; Jeff M Milunsky; Raveen Basran; Blake Papsin; Tracy L Stockley; Stephen W Scherer; Sanaa Choufani; Michael Brudno; Rosanna Weksberg
Journal:  Am J Hum Genet       Date:  2017-05-04       Impact factor: 11.025

  3 in total

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