扩展克莱夫斯特拉综合征的表型:103 人的言语、语言和认知能力。

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth Palmer, Adam P Vogel, Frederique Liegeois, Amanda Brignell, Siddharth Srivastava, Zoe Frazier, Di Milnes, Himanshu Goel, David J Amor, Ingrid E Scheffer, Tjitske Kleefstra, Angela T Morgan
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引用次数: 0

摘要

目的:言语和语言障碍是神经发育遗传病克莱夫斯特拉综合征的核心特征。目前尚未对交流能力进行系统研究,以指导干预建议。我们定义了一大批克莱夫斯特拉综合征患者的言语、语言和认知表型谱系:方法:纳入 103 名克莱夫斯特拉综合征患者(40 名男性,中位年龄为 9.5 岁,范围为 1-43 岁),这些患者均存在致病变异(52 例 9q34.3 缺失,50 例基因内变异,1 例平衡易位)。对患者的言语、语言和非语言沟通能力进行了评估。此外,还获得了认知、健康和神经发育方面的数据:认知能力范围从智力一般(12/79,15%)到重度智障(12/79,15%)不等。语言能力也从智力一般(10/90,11%)到严重智障(53/90,59%)不等。48/49(98%)名言语障碍者出现了言语障碍,甚至与一般的语言和认知能力同时出现。有 11/80 例(14%)患者在运动、语言和社会心理方面出现发育倒退。对于 61/103 例(59%)患者来说,手语和语言生成器等交流辅助工具至关重要,其中包括那些言语能力极弱、有语言障碍或正在退步的患者:结论:克莱夫斯特拉综合征的言语、语言和认知特征非常广泛,从严重障碍到能力一般不等。基因型和年龄并不能解释表型的变化。尽早使用交流辅助工具可改善交流和生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals.

Objectives: Speech and language impairments are core features of the neurodevelopmental genetic condition Kleefstra syndrome. Communication has not been systematically examined to guide intervention recommendations. We define the speech, language and cognitive phenotypic spectrum in a large cohort of individuals with Kleefstra syndrome.

Method: 103 individuals with Kleefstra syndrome (40 males, median age 9.5 years, range 1-43 years) with pathogenic variants (52 9q34.3 deletions, 50 intragenic variants, 1 balanced translocation) were included. Speech, language and non-verbal communication were assessed. Cognitive, health and neurodevelopmental data were obtained.

Results: The cognitive spectrum ranged from average intelligence (12/79, 15%) to severe intellectual disability (12/79, 15%). Language ability also ranged from average intelligence (10/90, 11%) to severe intellectual disability (53/90, 59%). Speech disorders occurred in 48/49 (98%) verbal individuals and even occurred alongside average language and cognition. Developmental regression occurred in 11/80 (14%) individuals across motor, language and psychosocial domains. Communication aids, such as sign and speech-generating devices, were crucial for 61/103 (59%) individuals including those who were minimally verbal, had a speech disorder or following regression.

Conclusions: The speech, language and cognitive profile of Kleefstra syndrome is broad, ranging from severe impairment to average ability. Genotype and age do not explain the phenotypic variability. Early access to communication aids may improve communication and quality of life.

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来源期刊
Journal of Medical Genetics
Journal of Medical Genetics 医学-遗传学
CiteScore
7.60
自引率
2.50%
发文量
92
审稿时长
4-8 weeks
期刊介绍: Journal of Medical Genetics is a leading international peer-reviewed journal covering original research in human genetics, including reviews of and opinion on the latest developments. Articles cover the molecular basis of human disease including germline cancer genetics, clinical manifestations of genetic disorders, applications of molecular genetics to medical practice and the systematic evaluation of such applications worldwide.
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