Penner K A, Johnston J, Faircloth B H, Irish P, Williams C A
Tacachale Center, Department of Audiology, University Medical Center, Jacksonville, Florida.
Am J Med Genet. 1993 Apr 1;46(1):34-9. doi: 10.1002/ajmg.1320460108.
Persons with Angelman syndrome (AS) have mental retardation, epilepsy, and a characteristic "puppet-like" gait. Behaviorally, they are distinctive because they have no speech and have excessive laughter. A speech and communication evaluation of 7 persons with AS was performed to provide improved understanding of the speech deficit. Assessments included prelanguage and language development, oral motor abilities, and cognitive and social interaction skills. Results indicate that the typical lack of speech may not be due to mental retardation alone. Oral motor dyspraxia, and deficits in social interaction and attention were characteristic of AS and contributed to the lack of speech.
患有天使综合征(AS)的人存在智力障碍、癫痫以及典型的“木偶样”步态。在行为方面,他们很独特,因为不会说话且经常过度发笑。对7名患有天使综合征的人进行了言语和沟通评估,以增进对言语缺陷的理解。评估内容包括前语言和语言发展、口腔运动能力以及认知和社交互动技能。结果表明,典型的言语缺失可能并非仅由智力障碍导致。口腔运动性失用症以及社交互动和注意力方面的缺陷是天使综合征的特征,也是导致言语缺失的原因。