Suppr超能文献

一种由错义变异导致的、与赛-巴伯-比塞克-杨-辛普森综合征和生殖器髌骨综合征不同的表型的描述。

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

作者信息

Nishimura Naoto, Enomoto Yumi, Kumaki Tatsuro, Murakami Hiroaki, Ikeda Azusa, Goto Tomohide, Kurosawa Kenji

机构信息

Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.

Department of Pediatrics, National Defense Medical College, Tokorozawa, Japan.

出版信息

Mol Syndromol. 2022 May;13(3):221-225. doi: 10.1159/000520134. Epub 2022 Feb 2.

Abstract

Say-Barber-Biesecker-Young-Simpson syndrome (SBBYSS) and genitopatellar syndrome (GPS) are caused by variants of lysine acetyltransferase 6B (). These variants tend to occur in the terminal exons of . 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 . The patient showed a phenotype differing from those of SBBYSS and GPS. We also report patients with missense variants in the proximal exons of showing dysmorphic features and autistic behavior not resembling the characteristics of SBBYSS and GPS. Missense variants in the proximal exons of may have a dominant negative effect or cause gain of function, leading to unique phenotypes not resembling those of SBBYSS and GPS.

摘要

赛-巴伯-比塞克-杨-辛普森综合征(SBBYSS)和生殖器髌骨综合征(GPS)由赖氨酸乙酰转移酶6B(KAT6B)的变异引起。这些变异倾向于出现在KAT6B的末端外显子中。在此,我们报告一名患者,其因KAT6B外显子7中的一个新型错义变异而出现全球发育迟缓、智力残疾、自闭症行为、肌张力减退、面部畸形和癫痫发作。该患者表现出与SBBYSS和GPS不同的表型。我们还报告了KAT6B近端外显子存在错义变异的患者,他们表现出畸形特征和自闭症行为,与SBBYSS和GPS的特征不同。KAT6B近端外显子中的错义变异可能具有显性负效应或导致功能获得,从而导致与SBBYSS和GPS不同的独特表型。

相似文献

6
Clinical heterogeneity of polish patients with KAT6B-related disorder.波兰 KAT6B 相关障碍患者的临床异质性。
Mol Genet Genomic Med. 2023 Dec;11(12):e2265. doi: 10.1002/mgg3.2265. Epub 2023 Sep 1.

本文引用的文献

4
Facial Expression Production in Autism: A Meta-Analysis.自闭症患者的面部表情生成:一项荟萃分析。
Autism Res. 2018 Dec;11(12):1586-1601. doi: 10.1002/aur.2037. Epub 2018 Nov 4.
9
Further delineation of the KAT6B molecular and phenotypic spectrum.KAT6B分子和表型谱的进一步描绘。
Eur J Hum Genet. 2015 Sep;23(9):1165-70. doi: 10.1038/ejhg.2014.248. Epub 2014 Nov 26.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验