Sleep in Neurodevelopmental Disorders

Sleep in Neurodevelopmental Disorders
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DOI:
10.1016/bs.irrdd.2016.07.005
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发表时间:
2016-01-01
期刊:
INTERNATIONAL REVIEW OF RESEARCH IN DEVELOPMENTAL DISABILITIES, VOL 51
影响因子:
--
通讯作者:
Schwichtenberg, A. J.
Schwichtenberg, A. J.
中科院分区:
其他
文献类型:
--
作者:
Esbensen, A. J.;Schwichtenberg, A. J.

文献摘要

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患有智力和发育障碍(IDD)的人比普通人群经历更高的睡眠问题。虽然IDD患者是一个异质性群体,但一些睡眠问题集中在遗传综合征或疾病中。本文综述了Angelman综合征、科尔内利亚德兰格综合征、Cri du Chat综合征、唐氏综合征、脆性X综合征、Prader-Willi综合征、Smith-Magenis综合征、威廉姆斯综合征、自闭症谱系障碍和特发性IDD患者的睡眠问题的患病率。与睡眠问题相关的因素和睡眠治疗的证据进行审查,为每一个神经发育障碍。本文综述了神经发育障碍的睡眠研究进展,包括定义和测量睡眠问题的一致性,研究设计和结果报告的考虑因素,以及评估睡眠治疗时的考虑因素。
Individuals with intellectual and developmental disabilities (IDD) experience sleep problems at higher rates than the general population. Although individuals with IDD are a heterogeneous group, several sleep problems cluster within genetic syndromes or disorders. This review summarizes the prevalence of sleep problems experienced by individuals with Angelman syndrome, Cornelia de Lange syndrome, Cri du Chat syndrome, Down syndrome, fragile X syndrome, Prader-Willi syndrome, Smith-Magenis syndrome, Williams syndrome, autism spectrum disorder, and idiopathic IDD. Factors associated with sleep problems and the evidence for sleep treatments are reviewed for each neurodevelopmental disorder. Sleep research advancements in neurodevelopmental disorders are reviewed, including the need for consistency in defining and measuring sleep problems, considerations for research design and reporting of results, and considerations when evaluating sleep treatments.