Karla Guerrero-Leiva , Carme Brun-Gasca , Albert Fornieles-Deu , Ariadna Ramírez-Mallafrè
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引用次数: 0
Abstract
Introduction
Angelman syndrome (AS) is a rare condition with low prevalence associated with severe global developmental delay, behavioral phenotype of happy appearance and social interaction, moderate to severe intellectual disability with minimal or absent oral language associated with molecular etiology and featuring clinical variables.
Objectives
To describe communication and language abilities in a sample of individuals with AS from Spain and Portugal, explore the influence of molecular etiology, age and use of Augmentative and Alternative Communication (AAC).
Materials and methods
The sample comprised 40 individuals diagnosed with AS, from the Iberian Peninsula, assessed using the MacArthur Communicative Development Inventories.
Results
A characteristic profile is shown with a predominance of gestures and receptive language over expressive. Differences are noted by molecular subtype, age, use of AAC and the origin in the Iberian Peninsula.
Conclusions
The linguistic phenotype for Angelman Syndrome is consistent with findings from other studies, however associated variables such as molecular etiology and use of AAC should be considered.
导言:安格尔曼综合征(Angelman Syndrome,AS)是一种罕见的疾病,发病率低,伴有严重的全面发育迟缓、快乐外表和社会交往的行为表型、中度至重度智力障碍,口语极少或缺失,与分子病因学和特征性临床变量有关。目的描述西班牙和葡萄牙 AS 患者的交流和语言能力,探讨分子病因学、年龄和使用辅助和替代性交流(AAC)的影响。结论安杰尔曼综合症的语言表型与其他研究结果一致,但应考虑分子病因学和使用辅助交流设备等相关变量。