Rodrigues Filipe Brogueira, Wild Edward J
Huntington's Disease Centre, Institute of Neurology, University College London, London, UK.
Pract Neurol. 2016 Dec;16(6):452-454. doi: 10.1136/practneurol-2016-001423. Epub 2016 Jun 21.
Huntington's disease (HD) is a neurodegenerative condition characterised by motor dysfunction with involuntary movements and loss of voluntary control, cognitive deterioration and psychiatric problems. We report a 51-year-old man with early HD who experienced stereotyped episodes of repetitive, purposeless complex movements and unresponsiveness. His neurological examination was compatible with HD as were all investigations. We diagnosed psychogenic non-epileptic seizures. While seizures are common in juvenile-onset HD, they are no more prevalent in adult-onset HD than in the general population. However, neuropsychiatric symptoms are common in HD and can involve a number of different complaints. Patients may experience dissociative attacks soon after manifesting a HD diagnosis. Such episodes can be managed with patient and carer education, cognitive behavioural therapy and anxiolytic selective serotonin reuptake inhibitors.
亨廷顿舞蹈症(HD)是一种神经退行性疾病,其特征为伴有不自主运动的运动功能障碍、自主控制能力丧失、认知衰退和精神问题。我们报告了一名51岁的早期HD男性患者,他经历了重复性、无目的复杂运动和无反应性的刻板发作。他的神经系统检查与HD相符,所有检查结果也是如此。我们诊断为精神性非癫痫性发作。虽然癫痫发作在青少年型HD中很常见,但在成人型HD中并不比普通人群更普遍。然而,神经精神症状在HD中很常见,可能涉及多种不同的症状。患者在被诊断为HD后不久可能会出现分离性发作。此类发作可通过对患者及其护理人员的教育、认知行为疗法和抗焦虑选择性5-羟色胺再摄取抑制剂进行处理。