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伴有痴呆的遗传性痉挛性截瘫

Hereditary spastic paraplegia with dementia.

作者信息

Pridmore S, Rao G, Abusah P

机构信息

Department of Psychological Medicine, Royal Hobart Hospital, Tasmania.

出版信息

Aust N Z J Psychiatry. 1995 Dec;29(4):678-82. doi: 10.3109/00048679509064985.

Abstract

OBJECTIVE

Hereditary spastic paraplegia (HSP) with dementia is a very rare condition. The aim of the paper is to present the first report of HSP in a Fijian Indian family.

METHOD

A psychiatrist and a general physician examined the affected members of the family on five occasions over three years.

RESULTS

There are three affected individuals in a sibship of seven. The parents are without symptoms and the marriage is non-consanguineous. The course of the disease has been remarkably similar. All subjects were healthy and performing well in the early years of school. In two, symptoms of cognitive loss preceded difficulty with ambulation and in the third, these symptoms appeared concurrently. All subjects had both symptoms by 13 years of age; they were unable to ambulate independently by the mid to late teens, at which time there was dysarthria spastic paraplegia and dementia. One subject suffered a three month episode of hypomanic behaviour. Over the three-year study period deterioration was slight but noticeable.

CONCLUSIONS

It is possible that HSP is more commonly associated with pre-senile dementia than is currently recognised. HSP with dementia is a very rare cause of failing school performance. Physical examination of the patient and other family members is indicated if this diagnosis is being considered.

摘要

目的

伴有痴呆的遗传性痉挛性截瘫(HSP)是一种非常罕见的病症。本文旨在首次报道一个斐济裔印度家庭中的HSP病例。

方法

一名精神科医生和一名全科医生在三年时间里对该家庭的患病成员进行了五次检查。

结果

在一个七口之家的兄弟姐妹中有三人患病。父母无症状,且婚姻为非近亲婚姻。疾病进程非常相似。所有受试者在早年时都很健康且表现良好。其中两人在出现行走困难之前就有认知能力丧失的症状,第三人则同时出现这些症状。所有受试者在13岁时都出现了这两种症状;到青少年中后期,他们无法独立行走,此时出现了构音障碍、痉挛性截瘫和痴呆。一名受试者有为期三个月的轻躁狂行为发作。在三年的研究期间,病情恶化轻微但明显。

结论

HSP与早老性痴呆的关联可能比目前所认识到的更为常见。伴有痴呆的HSP是学业成绩下降的一种非常罕见的原因。如果考虑作出这一诊断,应对患者及其他家庭成员进行体格检查。

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