Department of Psychology, Case Western Reserve University, Cleveland, OH, USA.
Neuropsychiatr Dis Treat. 2010 May 6;6:107-18. doi: 10.2147/ndt.s5560.
Prader-Willi syndrome (PWS) is a complex neurodevelopmental disorder caused by an abnormality on the long arm of chromosome 15 (q11-q13) that results in a host of phenotypic characteristics, dominated primarily by hyperphagia and insatiable appetite. Characteristic behavioral disturbances in PWS include excessive interest in food, skin picking, difficulty with a change in routine, temper tantrums, obsessive and compulsive behaviors, and mood fluctuations. Individuals with PWS typically have intellectual disabilities (borderline to mild/moderate mental retardation) and exhibit a higher overall behavior disturbance compared to individuals with similar intellectual disability. Due to its multisystem disorder, family members, caregivers, physicians, dieticians, and speech-language pathologists all play an important role in the management and treatment of symptoms in an individual with PWS. This article reviews current research on behavior and cognition in PWS and discusses management guidelines for this disorder.
普拉德-威利综合征(PWS)是一种复杂的神经发育障碍,由 15 号染色体长臂(q11-q13)的异常引起,导致多种表型特征,主要表现为食欲过盛和无法满足的食欲。PWS 的典型行为障碍包括对食物过度关注、皮肤搔抓、难以适应常规变化、发脾气、强迫和强迫行为以及情绪波动。患有 PWS 的个体通常存在智力障碍(边缘型至轻度/中度智力障碍),并且与具有相似智力障碍的个体相比,表现出更高的整体行为障碍。由于其多系统障碍,家庭成员、照顾者、医生、营养师和言语语言病理学家在个体 PWS 的症状管理和治疗中都发挥着重要作用。本文综述了 PWS 行为和认知的当前研究,并讨论了该障碍的管理指南。