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Delineation of a Phenotype Caused by a KAT6B Missense Variant Not Resembling Say-Barber-Biesecker-Young-Simpson and Genitopatellar Syndromes.
Nishimura, Naoto; Enomoto, Yumi; Kumaki, Tatsuro; Murakami, Hiroaki; Ikeda, Azusa; Goto, Tomohide; Kurosawa, Kenji.
Afiliación
  • Nishimura N; Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
  • Enomoto Y; Department of Pediatrics, National Defense Medical College, Tokorozawa, Japan.
  • Kumaki T; Clinical Research Institute, Kanagawa Children's Medical Center, Yokohama, Japan.
  • Murakami H; Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
  • Ikeda A; Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
  • Goto T; Department of Neurology, Kanagawa Children's Medical Center, Yokohama, Japan.
  • Kurosawa K; Department of Neurology, Kanagawa Children's Medical Center, Yokohama, Japan.
Mol Syndromol ; 13(3): 221-225, 2022 May.
Article en En | MEDLINE | ID: mdl-35707592
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Syndromol Año: 2022 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Syndromol Año: 2022 Tipo del documento: Article País de afiliación: Japón
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