• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

新生儿缺氧缺血性脑病导致严重智力发育迟缓及运动障碍患者后遗症的长期临床病程

[Long-term clinical course of sequelae in patients with neonatal anoxic encephalopathy resulting in profound mental retardation and motor disturbance].

作者信息

Ishizaki A, Kubota M, Fueki N, Shinozaki M, Kurata K, Takei M, Sakamoto K

机构信息

Metropolitan Medical Center of the Severely Handicapped, Fuchu, Tokyo.

出版信息

No To Hattatsu. 1993 Jan;25(1):26-32.

PMID:8416692
Abstract

A long-term observation has been made in 58 patients (30 males and 28 females) with severe sequelae of neonatal anoxic encephalopathy. They aged from 8 months to 65 years. All of them had motor disturbances and profound mental retardation. Motor function was improved in 4 patients with aging. In contrast, motor activity deteriorated in 11 cases, of which 4 showed a mental regression. Among them, patients who had originally better motor ability than sitting were likely to deteriorate by uncontrollable epilepsy and/or excessive administration of anticonvulsants. Regression of the patients with worse motor ability like bedridden appeared to attributable hypertonia of muscles and bodily deformation. Fifteen cases showed an exacerbation of general condition which originated predominantly to respiratory distress. Twelve patients died including 6 exacerbated cases. Exacerbation or death may have occurred frequently in specific periods of infancy, adolescence and youth with the patients who showed very low motor function such as bedridden and no locomotion.

摘要

对58例(男30例,女28例)新生儿缺氧缺血性脑病重度后遗症患者进行了长期观察。他们的年龄从8个月到65岁不等。所有患者均有运动障碍和重度智力发育迟缓。4例患者随着年龄增长运动功能有所改善。相比之下,11例患者运动活动恶化,其中4例出现智力倒退。其中,原本运动能力优于坐位的患者可能因无法控制的癫痫发作和/或抗惊厥药物使用过量而恶化。运动能力较差如卧床不起的患者病情倒退似乎归因于肌肉张力亢进和身体变形。15例患者全身状况恶化,主要源于呼吸窘迫。12例患者死亡,其中6例为病情恶化病例。在婴儿期、青春期和青年期的特定阶段,对于运动功能极低如卧床不起且无法活动的患者,病情恶化或死亡可能经常发生。

相似文献

1
[Long-term clinical course of sequelae in patients with neonatal anoxic encephalopathy resulting in profound mental retardation and motor disturbance].新生儿缺氧缺血性脑病导致严重智力发育迟缓及运动障碍患者后遗症的长期临床病程
No To Hattatsu. 1993 Jan;25(1):26-32.
2
[A clinical study of death in profound mental retardation with motor disturbance].[重度智力发育迟缓伴运动障碍患者死亡情况的临床研究]
No To Hattatsu. 1990 Jul;22(4):357-63.
3
[Incidence rate of cerebral palsy, severe mental and motor retardation, and mental retardation in a suburban Tokyo area].[东京郊区脑瘫、重度智力与运动发育迟缓以及智力发育迟缓的发病率]
No To Hattatsu. 1991 Sep;23(5):481-5.
4
[Perinatal asphyxia, hypoxic-ischemic encephalopathy and neurological sequelae in full-term newborns. II. Description and interrelation].[足月新生儿的围产期窒息、缺氧缺血性脑病及神经后遗症。II. 描述与相互关系]
Rev Neurol. 1996 Aug;24(132):969-76.
5
Thiamine deficiency in infancy: long-term follow-up.婴儿期硫胺素缺乏症:长期随访
Pediatr Neurol. 2014 Sep;51(3):311-6. doi: 10.1016/j.pediatrneurol.2014.05.010. Epub 2014 May 15.
6
[Incidence rates of cerebral palsy, severe mental and motor retardation, and Down syndrome in the city of Kokubunji in suburban Tokyo].[东京郊区国分寺市脑瘫、严重智力和运动发育迟缓以及唐氏综合征的发病率]
No To Hattatsu. 1993 Jan;25(1):16-20.
7
Apparent life threatening events with serious sequelae in infants and young children.婴幼儿期具有严重后遗症的明显危及生命事件。
J Paediatr Child Health. 1992 Apr;28(2):151-5. doi: 10.1111/j.1440-1754.1992.tb02631.x.
8
[A clinical study of severely mental and motor retarded children].[重度智力和运动发育迟缓儿童的临床研究]
No To Hattatsu. 1994 Jan;26(1):20-5.
9
[Delayed motor and intellectual sequelae in 34 children with cerebral palsy and CT signs of periventricular leukomalacia].34例脑性瘫痪合并脑室周围白质软化CT征象患儿的迟发性运动和智力后遗症
Ann Pediatr (Paris). 1987 Oct;34(8):615-21.
10
Long-term outcomes in motor and cognitive impairment with acute encephalopathy.急性脑病所致运动和认知障碍的长期预后
Brain Dev. 2018 Oct;40(9):807-812. doi: 10.1016/j.braindev.2018.05.013. Epub 2018 Jun 8.