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A longitudinal perspective on the pharmacotherapy of 24 adult patients with Phelan McDermid syndrome.对24例成年费兰-麦克德米德综合征患者药物治疗的纵向观察。
Eur J Med Genet. 2020 Mar;63(3):103751. doi: 10.1016/j.ejmg.2019.103751. Epub 2019 Aug 27.
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Retrospective chart review of catatonia in child and adolescent psychiatric patients.回顾性图表分析儿童和青少年精神科患者的紧张症。
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紧张症:自闭症晚期退化的常见原因

Catatonia: A Common Cause of Late Regression in Autism.

作者信息

Ghaziuddin Mohammad

机构信息

Department of Psychiatry, University of Michigan, Ann Arbor, MI, United States.

出版信息

Front Psychiatry. 2021 Oct 28;12:674009. doi: 10.3389/fpsyt.2021.674009. eCollection 2021.

DOI:10.3389/fpsyt.2021.674009
PMID:34777033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8585308/
Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by social communication deficits and restricted interests and behaviors which begin very early in life. In about a quarter of cases, the symptoms emerge about 18-24 months after a period of normal development, a phenomenon commonly described as early regression. However, marked functional decline can also occur in persons with autism after a relatively stable childhood. As opposed to early regression, which occurs in normally developing children, late regression occurs typically in adolescents with an established diagnosis of autism. Apart from their occasional mention in the literature, these individuals have not been examined systematically. This Brief Report describes the presentation, comorbidity and short-term outcome of 20 persons with ASD who developed late regression. The mean age of onset of regression was 13 years. One of the earliest symptoms was an increase in obsessive slowing and compulsive rituals. Other symptoms included motor abnormalities, aggression and mood disturbance. The most common comorbid disorder was catatonia occurring in 17 patients. Despite treatment with several modalities, the outcome was often suboptimal. These findings suggest that catatonia is a common cause of late regression in persons with autism. Clinical and research implications are discussed.

摘要

自闭症谱系障碍(ASD)是一种神经发育障碍,其特征是社交沟通缺陷以及兴趣和行为受限,这些症状在生命早期就会出现。在大约四分之一的病例中,症状会在一段正常发育时期后的18至24个月出现,这种现象通常被称为早期退化。然而,在童年相对稳定之后,自闭症患者也可能出现明显的功能衰退。与发生在正常发育儿童中的早期退化不同,晚期退化通常发生在已确诊自闭症的青少年中。除了在文献中偶尔被提及外,这些个体尚未得到系统研究。本简要报告描述了20例出现晚期退化的自闭症谱系障碍患者的临床表现、共病情况和短期预后。退化的平均发病年龄为13岁。最早出现的症状之一是强迫性动作迟缓及强迫仪式行为增加。其他症状包括运动异常、攻击行为和情绪障碍。最常见的共病是紧张症,17例患者出现该症状。尽管采用了多种治疗方式,预后往往并不理想。这些发现表明,紧张症是自闭症患者晚期退化的常见原因。本文还讨论了临床和研究意义。