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史密斯-马吉尼斯综合征的行为障碍及治疗策略

Behavioral disturbance and treatment strategies in Smith-Magenis syndrome.

作者信息

Poisson Alice, Nicolas Alain, Cochat Pierre, Sanlaville Damien, Rigard Caroline, de Leersnyder Hélène, Franco Patricia, Des Portes Vincent, Edery Patrick, Demily Caroline

机构信息

Center for Screening and Treatment of Psychiatric Disorders of Genetic Origin, Vinatier Hospital, 95 Bd Pinel, 69678, Lyon, France.

Cognitive Neuroscience Center, UMR 5229, French National Research Center (CNRS), Bron, France.

出版信息

Orphanet J Rare Dis. 2015 Sep 4;10:111. doi: 10.1186/s13023-015-0330-x.

Abstract

BACKGROUND

Smith-Magenis syndrome is a complex neurodevelopmental disorder that includes intellectual deficiency, speech delay, behavioral disturbance and typical sleep disorders. Ninety percent of the cases are due to a 17p11.2 deletion encompassing the RAI1 gene; other cases are linked to mutations of the same gene. Behavioral disorders often include outbursts, attention deficit/hyperactivity disorders, self-injury with onychotillomania and polyembolokoilamania (insertion of objects into body orifices), etc. Interestingly, the stronger the speech delay and sleep disorders, the more severe the behavioral issues. Sleep disturbances associate excessive daytime sleepiness with nighttime agitation. They are underpinned by an inversion of the melatonin secretion cycle. However, the combined intake of beta-blockers in the morning and melatonin in the evening may radically alleviate the circadian rhythm problems.

DISCUSSION

Once sleep disorders are treated, the next challenge is finding an effective treatment for the remaining behavioral problems. Unfortunately, there is a lack of objective guidelines. A comprehensive evaluation of such disorders should include sleep disorders, potential causes of pain, neurocognitive level and environment (i.e. family and school). In any case, efforts should focus on improving communication skills, identifying and treating attention deficit/hyperactivity, aggressiveness and anxiety. Treatment of Smith-Magenis syndrome is complex and requires a multidisciplinary team including, among others, geneticists, psychiatrists, neuropediatricians/neurologists, somnologists, developmental and behavioral pediatricians, and speech and language therapists.

摘要

背景

史密斯-马吉尼斯综合征是一种复杂的神经发育障碍,包括智力缺陷、语言发育迟缓、行为障碍和典型的睡眠障碍。90%的病例是由于17号染色体短臂11.2区缺失,该区域包含RAI1基因;其他病例与同一基因的突变有关。行为障碍通常包括爆发性发作、注意力缺陷/多动障碍、拔甲癖和异物插入癖(将物体插入身体孔窍)等自我伤害行为。有趣的是,语言发育迟缓和睡眠障碍越严重,行为问题就越严重。睡眠障碍表现为白天过度嗜睡和夜间烦躁不安。它们是由褪黑素分泌周期的倒置所导致的。然而,早上联合服用β受体阻滞剂和晚上服用褪黑素可能会从根本上缓解昼夜节律问题。

讨论

一旦睡眠障碍得到治疗,下一个挑战就是为剩余的行为问题找到有效的治疗方法。不幸的是,目前缺乏客观的指导方针。对这些障碍的全面评估应包括睡眠障碍、潜在的疼痛原因、神经认知水平和环境(即家庭和学校)。无论如何,应努力提高沟通技巧,识别和治疗注意力缺陷/多动、攻击性和焦虑问题。史密斯-马吉尼斯综合征的治疗很复杂,需要一个多学科团队,其中包括遗传学家、精神科医生、神经儿科医生/神经科医生、睡眠专家、发育和行为儿科医生以及言语和语言治疗师。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/382f/4559928/f39e6e0add80/13023_2015_330_Fig1_HTML.jpg

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