期刊文献+

Fahr病合并家族性烟雾病1例

Fahr's disease complicated with familial moyamoya disease: a case report
原文传递
导出
摘要 Fahr病是一种表现为双侧基底节区或小脑齿状核钙化的罕见神经变性疾病,早期无明显不适,中晚期可缓慢出现肌张力障碍、认知功能减退、言语欠清、共济失调、震颤麻痹及精神行为异常等症状[1],其临床表现可能与钙化部位、钙化程度以及脑功能回路改变有关[2]。Fahr病的确切发病机制尚不完全清楚,钙化可能是转移性沉积,继发于局部血脑屏障破坏或钙磷代谢紊乱[3]。烟雾病是一种原因不明的慢性进行性脑血管闭塞性疾病,主要表现为单侧或双侧颈内动脉远端、大脑中动脉及大脑前动脉近端狭窄或闭塞伴脑底部和软脑膜烟雾状细小血管形成;大部分病例为散发性,但也可为家族遗传性[4,5]。目前关于Fahr病合并烟雾病鲜有报道,现报道1例。
作者 马召玺 岳雨珊 高福秋 罗艳 曹勇军 肖国栋 Ma Zhaoxi;Yue Yushan;Gao Fuqiu;Luo Yan;Cao Yongjun;Xiao Guodong(Department of Neurology,Kunshan First People's Hospital,Kunshan 215300,China;Department of Neurorehabilitation,Kunshan Rehabilitation Hospital,Kunshan 215300,China;Department of Neurology,the Second Affiliated Hospital of Soochow University,Suzhou 215314,China)
出处 《国际脑血管病杂志》 2019年第8期638-640,共3页 International Journal of Cerebrovascular Diseases
  • 相关文献

参考文献3

二级参考文献71

  • 1段炼,孙伟建,王芙昱,李生,杨伟中,孔繁文.国人烟雾病临床特征探讨[J].中国临床神经外科杂志,2005,10(4):269-271. 被引量:75
  • 2杨新宇,杨树源.Moyamoya病的手术治疗[J].中华神经外科杂志,2007,23(3):239-240. 被引量:8
  • 3Horn P, Vajkoczy P, Schmiedek P. Die spontane okklusion des cir?culus arteriosus Willisii (Moyamoya-Erkrankung). Diagnostik und trerapie[J]. Der Nervenarzt, 2001, 72: 406.
  • 4Kuriyama S, Kusaka Y ,Fujimura M, et al. Prevalence and clinicoepi?demiological features of Moyamoya disease inJapan: findings from a nationwide epidemiological survey[J] . Stroke ,2008 ,39 :42.
  • 5Fukui M. Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis (Moyamoya disease). Research committee on spontaneous occlusion of the circle of Willis (Moy?amoya disease) of the ministry of health and welfare,Japan[J] . Clin Neurol Neurosurg, 1997,99 (SuppI2): S238.
  • 6Seol HJ, Wang KC, Kim SK, et al. Familial occurrence of Moy?amoya disease: a clinical study[J]. Childs N erv Syst, 2006, 22: 1143.
  • 7Wakai K, Tamakoshi A, Lkezaki K, et al. Epidemiologieal features of Moyamoya disease inJapan: findings from a nationwide survey[J]. Clin Neurol Neurosurg, 1997,99 (Suppl Zj , S1.
  • 8YeonJY, Shin HJ, Kong DS, et al. The prediction of contralateral progression in children and adolescents with unilateral Moyamoya disease[J]. Stroke, 2011 , 42: 2973.
  • 9Park EK, Lee YH, Shim KW, et al. Natural history and progression factors of unilateral Moyamoya disease in pediatric patients[J] . Childs Nerv Syst , 2011 , 27: 1281.
  • 10Yamauchi T, Mitsuhiro T, Kiyohiro H, et al. Linkage of familial Moyamoya disease (spontaneous occlusion of the circle of the Wil?lis) to chromosome 17 q25[J] . Stroke, 2000, 31 : 930.

共引文献19

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部