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面部起病的感觉运动神经元病一例 被引量：8

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摘要 面部起病的感觉运动神经元病（又称FOSMN综合征）以三叉神经支配区域的感觉障碍起病，继而出现下运动神经元损害国内尚未查阅到相关文献，现将我院近来诊治的1例报道如下.
作者 唐一麟 朱雯华 齐凯 程忻 赵重波 陈嬿 王亮 卢家红
机构地区 复旦大学附属华山医院神经内科
出处 《中华神经科杂志》 CAS CSCD 北大核心 2013年第10期715-716,共2页 Chinese Journal of Neurology
关键词 运动神经元病 感觉障碍 面部 运动神经元损害 三叉神经支 综合征
分类号 R744.8 [医药卫生—神经病学与精神病学]
  • 相关文献

参考文献6

  • 1Vueie S, Tian D, Chong PS, et al. Facial onset sensory and motor neurnnopathy ( FOSMN syndrome) : a novel syndrome in neurology+. Brain, 2006, 129 ( Pt 12 ) : 3384-3390.
  • 2lsoardo G, Troni W. Sporadic bulhospinal muscle atrophy with ta.cial-onset sensory neuropathy. Muscle Nerve, 2008, 37: 659-662.
  • 3Hokonohara T, Shigeto H, Kawano Y, et al. Facial onset sensory and motor neuronopathy (FOSMN) syndrome responding to immunotherapies. J Neurol Sci, 2008, 275: 157-158.
  • 4Fluchere F, Verschueren A, Cintas P, et al. Clinical features and follow-up of four new cases of facial-onset sensory and motor neuronopathy. Muscle Nerve, 2011 , 43: 136-140.
  • 5Vucic S, Stein TD, Hedley-Whyte ET, et al. FOSMN syndrome: novel insight into disease pathophysiology. Neurology, 2012, 79:73 -79.
  • 6Dobrev D, Barhon R J, Anderson NE, et al. Facial onset sensorimotor neuronopathy syndrome: a case series. J Clin Neuromuscul Dis, 2012, 14: 7-10.

同被引文献23

  • 1唐海燕,罗苏珊,曹文杰.面部起病的感觉运动神经元病一例[J].上海医学,2020,43(2):117-118. 被引量：1
  • 2Vucic S, Tian D, Chong PS, et al. Facial onset sensory and motor neuronopathy (FOSMN syndrome): a novel syndrome in neurology [J]. Brain, 2006, 129:3384-3390.
  • 3Vucic S, Stein TD, Hedley-Whyte ET, et al. FOSMN syndrome: novel insight into disease pathophysiology[J]. Neurology, 2012,79: 73-79.
  • 4Sonoda K, Sasaki K, Tateishi T, et al. TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: an autopsied case report and a review of the literature[J]. J Neurol Sci, 2013, 332:148-153.
  • 5Ziso B, Williams TL, Waiters R J, et al. Facial onset sensory and mo- tor neuronopathy: further evidence for a TDP-43 proteinopathy[J]. Case Rep Neurol, 2015, 7:95-100.
  • 6Dalla BE, Rigamonti A, Mantero V, et al. Heterozygous D9OA- SOD1 mutation in a patient with facial onset sensory motor neu- ronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral scle- rosis[J]. J Neurol Neurosurg Psychiatry, 2014, 85:1009-1011.
  • 7Felbecker A, Camu W, Valdmanis PN, et al. Four familial ALS ped- igrees discordant for two SOD1 mutations: are all SODI mutations pathogenic?[J]. J Neurol Neurosurg Psychiatry, 2010, 81:572-577.
  • 8Knopp M, Vaghela NN, Shanmugam SV, et al. Facial onset sensory motor neuronopathy: an immunoglobulin-responsive case[J]. J Clin Neuromuscul Dis, 2013, 14:176-179.
  • 9Fluchere F, Verschueren A, Cintas P, et al. Clinical features and follow-up of four new cases of facial-onset sensory and motor neu- ronopathy[J]. Muscle Nerve, 2011, 43:136-140.
  • 10Hokonohara T, Shigeto H, Kawano Y, et al. Facial onset sensory and motor neuronopathy (FOSMN) syndrome responding to immunother- apies[J]. J Neurol Sci, 2008, 275:157-158.

引证文献8

二级引证文献9

中华神经科杂志
2013年 第10期

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