• 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

In vivo diagnosis of Hallervorden-Spatz disease.

作者信息

Ostergaard J R, Christensen T, Hansen K N

机构信息

Department of Paediatrics, Aarhus Kommunehospital, University Hospital of Aarhus, Denmark.

出版信息

Dev Med Child Neurol. 1995 Sep;37(9):827-33. doi: 10.1111/j.1469-8749.1995.tb12066.x.

DOI:10.1111/j.1469-8749.1995.tb12066.x
PMID:7589865
Abstract

The authors present the MRI findings of two children with insidious walking difficulties, signs of corticospinal tract involvement, and signs and symptoms of extrapyramidal dysfunction such as rigidity and generalized dystonia, the latter with predominance of oromandibular involvement. In one child, MRI revealed prominent hypo-intensity in the globus pallidus and in the substantia nigra on T2-weighted spin echo images, consistent with iron deposition and thus with previous post-mortem findings of Hallervorden-Spatz disease. In the other case, the hypo-intensity was restricted to the globus pallidus, in which a small area of hyperintensity in its internal segment was demonstrated--the so called 'eye-of-the-tiger' sign. The authors propose that a combination of previously mentioned neurological signs with these specific MRI findings is highly suggestive of an in vivo diagnosis of the late infantile type of HSD.

摘要

相似文献

1
In vivo diagnosis of Hallervorden-Spatz disease.
Dev Med Child Neurol. 1995 Sep;37(9):827-33. doi: 10.1111/j.1469-8749.1995.tb12066.x.
2
Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life.
J Neurol. 1992 Oct;239(8):417-25. doi: 10.1007/BF00856805.
3
[The role of magnetic resonance imaging in the diagnosis of Hallervorden-Spatz disease].[磁共振成像在Hallervorden-Spatz病诊断中的作用]
Rinsho Shinkeigaku. 1990 Sep;30(9):972-7.
4
Familial pediatric rapidly progressive extrapyramidal syndrome: is it Hallervorden-Spatz disease?家族性小儿快速进展性锥体外系综合征:是苍白球黑质变性吗?
Pediatr Neurol. 2003 Aug;29(2):170-2. doi: 10.1016/s0887-8994(03)00231-5.
5
The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome.虎眼征并非哈勒沃登-施帕茨综合征的可靠疾病标志物。
Neuropediatrics. 2005 Jun;36(3):221-2. doi: 10.1055/s-2005-865714.
6
Hallervorden-Spatz syndrome and MRI: the "tiger's eye". One case.哈勒沃登-施帕茨综合征与磁共振成像:“虎眼征”。1例报告。
J Neuroradiol. 1993 Mar;20(1):70-5.
7
Hallervorden-Spatz disease.
Australas Radiol. 1996 Aug;40(3):351-3. doi: 10.1111/j.1440-1673.1996.tb00419.x.
8
[Contribution of nuclear magnetic imaging in the diagnosis of Hallervorden-Spatz syndrome].
Arch Fr Pediatr. 1993 Jan;50(1):35-7.
9
[Hallervorden Spatz syndrome: magnetic resonance findings. Case report].[苍白球黑质红核色素变性综合征:磁共振成像表现。病例报告]
Arq Neuropsiquiatr. 2004 Sep;62(3A):730-2. doi: 10.1590/s0004-282x2004000400031. Epub 2004 Aug 24.
10
MR imaging of a group I case of Hallervorden-Spatz disease.
J Comput Assist Tomogr. 1988 Sep-Oct;12(5):851-3. doi: 10.1097/00004728-198809010-00023.

引用本文的文献

1
Neurodegeneration associated with genetic defects in phospholipase A(2).与磷脂酶A(2)基因缺陷相关的神经退行性变
Neurology. 2008 Oct 28;71(18):1402-9. doi: 10.1212/01.wnl.0000327094.67726.28. Epub 2008 Sep 17.
2
Iron in neurodegenerative disorders.神经退行性疾病中的铁
Neurotox Res. 2002 Nov-Dec;4(7-8):637-653. doi: 10.1080/1029842021000045444.
3
Iron-induced susceptibility effect at the globus pallidus causes underestimation of flow and volume on dynamic susceptibility contrast-enhanced MR perfusion images.
铁诱导的苍白球敏感性效应导致动态对比增强磁共振灌注图像上血流和血容量的低估。
AJNR Am J Neuroradiol. 2002 Jun-Jul;23(6):1022-9.