DYT1型肌张力障碍的精神障碍

IF 1.3 Q4 NEUROSCIENCES
A. Yahya, Meena Naguib, Shakil Khawaja
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引用次数: 0

摘要

DYT1型肌张力障碍是一种罕见的遗传性儿童期肌张力障碍。精神合并症在肌张力障碍患者中增加。在这里,作者提出了一个25岁男性DYTI肌张力障碍的病例,之前接受过深部脑刺激治疗,在一次几乎致命的自杀未遂后引起了二级保健的注意。作者还总结了他们在文献检索中关于继发于DYT1基因的原发性肌张力障碍精神障碍的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Psychiatric disorder in DYT1 dystonia
DYT1 dystonia is a rare and genetically inherited childhood‐onset dystonia. Psychiatric comorbidity is increased in patients with dystonia. Here the authors present the case of a 25‐year‐old male with DYTI dystonia, previously treated with deep brain stimulation, who came to the attention of secondary care after a near fatal suicide attempt. The authors also summarise their findings from a literature search on psychiatric disorder in primary dystonia secondary to the DYT1 gene.
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来源期刊
CiteScore
1.70
自引率
8.30%
发文量
44
期刊介绍: Progress in Neurology and Psychiatry is published nine times a year, and is a journal for specialists in secondary care, GPs with an interest in neurology and psychiatry, community psychiatric nurses and other specialist healthcare professionals. Articles cover management, news updates and opinion in all areas of neurology and psychiatry.
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