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扩展 Kleefstra 综合征表型:103 例患者的言语、语言和认知功能。

Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals.

机构信息

Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.

Department of Audiology and Speech Pathology, The University of Melbourne, Melbourne, Victoria, Australia.

出版信息

J Med Genet. 2024 May 21;61(6):578-585. doi: 10.1136/jmg-2023-109702.

Abstract

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.

摘要

目的

言语和语言障碍是神经发育遗传疾病 Kleefstra 综合征的核心特征。尚未对沟通情况进行系统检查以指导干预建议。我们在 Kleefstra 综合征的大型患者队列中定义了言语、语言和认知表现谱。

方法

纳入了 103 名 Kleefstra 综合征患者(40 名男性,中位年龄 9.5 岁,范围 1-43 岁),他们均携带致病性变异(52 例 9q34.3 缺失,50 例基因内变异,1 例平衡易位)。评估了言语、语言和非言语沟通情况。获得了认知、健康和神经发育数据。

结果

认知谱从平均智力(12/79,15%)到严重智力障碍(12/79,15%)不等。语言能力也从平均智力(10/90,11%)到严重智力障碍(53/90,59%)不等。言语障碍发生在 49 名言语者中的 48 名(98%)中,甚至在伴有平均语言和认知能力的情况下也会发生。11 名个体(11/80,14%)在运动、语言和心理社会领域出现了发育倒退。包括言语障碍、有言语障碍或出现倒退的 61 名患者中的 103 名(59%)需要言语治疗辅助,例如手语和言语生成设备。

结论

Kleefstra 综合征的言语、语言和认知表现谱广泛,从严重受损到平均能力不等。基因型和年龄不能解释表型的可变性。早期使用沟通辅助工具可能会改善沟通和生活质量。

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