• 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

Taste loss as the sole presenting symptom in Chinese patient with facial onset sensory and motor neuronopathy.

作者信息

Chen Lu-Xi, Liu Gong-Lu, Yu Hao, Wu Zhi-Ying, Li Hong-Fu

机构信息

Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

CNS Neurosci Ther. 2021 Dec;27(12):1610-1613. doi: 10.1111/cns.13755. Epub 2021 Nov 2.

DOI:10.1111/cns.13755
PMID:34729923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8611768/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1493/8611768/1a284423f323/CNS-27-1610-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1493/8611768/1a284423f323/CNS-27-1610-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1493/8611768/1a284423f323/CNS-27-1610-g001.jpg

相似文献

1
Taste loss as the sole presenting symptom in Chinese patient with facial onset sensory and motor neuronopathy.味觉丧失作为中国面部起病的感觉和运动神经元病患者的唯一首发症状。
CNS Neurosci Ther. 2021 Dec;27(12):1610-1613. doi: 10.1111/cns.13755. Epub 2021 Nov 2.
2
Facial nuclear degeneration on MRI in bulbar onset amyotrophic lateral sclerosis.
QJM. 2013 Sep;106(9):875-6. doi: 10.1093/qjmed/hct104. Epub 2013 May 16.
3
Taste disorder in facial onset sensory and motor neuronopathy: a case report.面部运动感觉神经元病味觉障碍：病例报告。
BMC Neurol. 2020 Feb 29;20(1):71. doi: 10.1186/s12883-020-01639-x.
4
Optinurin inclusions in proximal hereditary motor and sensory neuropathy (HMSN-P): familial amyotrophic lateral sclerosis with sensory neuronopathy?
J Neurol Neurosurg Psychiatry. 2011 Dec;82(12):1299. doi: 10.1136/jnnp-2011-301240. Epub 2011 Sep 23.
5
Facial onset sensory motor neuronopathy (FOSMN) syndrome: an unusual amyotrophic lateral sclerosis phenotype?面部起病的感觉运动神经元病（FOSMN）综合征：一种不寻常的肌萎缩侧索硬化表型？
J Neurol Neurosurg Psychiatry. 2014 Sep;85(9):951. doi: 10.1136/jnnp-2014-307756. Epub 2014 Mar 18.
6
Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis.面部起始感觉运动神经元病（FOSMN）综合征患者中杂合 D90A-SOD1 突变：肌萎缩侧索硬化症的桥梁。
J Neurol Neurosurg Psychiatry. 2014 Sep;85(9):1009-11. doi: 10.1136/jnnp-2013-307416. Epub 2014 Mar 3.
7
Persistent bitter taste as an initial symptom of amyotrophic lateral sclerosis.持续性口苦作为肌萎缩侧索硬化症的初始症状
J Neurol Neurosurg Psychiatry. 2003 May;74(5):687-8. doi: 10.1136/jnnp.74.5.687-a.
8
Hypogeusia and hearing loss in a patient with an inferior collicular infarction.一名下丘梗死患者出现味觉减退和听力丧失。
Neurology. 2005 Dec 13;65(11):1840-1. doi: 10.1212/01.wnl.0000187083.90889.72.
9
Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?伴感觉神经病的肌萎缩侧索硬化症：多系统疾病的一部分？
J Neurol Neurosurg Psychiatry. 2007 Jul;78(7):750-3. doi: 10.1136/jnnp.2006.098798.
10
A nationwide survey of facial onset sensory and motor neuronopathy in Japan.日本全国性面部起病的感觉和运动神经元病调查。
J Neurol Sci. 2024 Apr 15;459:122957. doi: 10.1016/j.jns.2024.122957. Epub 2024 Mar 11.

引用本文的文献

1
Facial onset sensory and motor neuronopathy (FOSMN syndrome): Cases series and systematic review.面肌起始感觉运动神经元病（FOSMN 综合征）：病例系列和系统评价。
Neurol Sci. 2023 Jun;44(6):1969-1978. doi: 10.1007/s10072-023-06703-1. Epub 2023 Mar 3.

本文引用的文献

1
Facial Onset Sensory and Motor Neuronopathy: New Cases, Cognitive Changes, and Pathophysiology.面部起病的感觉和运动神经元病：新病例、认知改变及病理生理学
Neurol Clin Pract. 2021 Apr;11(2):147-157. doi: 10.1212/CPJ.0000000000000834.
2
Taste disorder in facial onset sensory and motor neuronopathy: a case report.面部运动感觉神经元病味觉障碍：病例报告。
BMC Neurol. 2020 Feb 29;20(1):71. doi: 10.1186/s12883-020-01639-x.
3
Neuro-Cells therapy improves motor outcomes and suppresses inflammation during experimental syndrome of amyotrophic lateral sclerosis in mice.
神经细胞疗法改善了实验性肌萎缩侧索硬化症小鼠的运动功能，并抑制了炎症反应。
CNS Neurosci Ther. 2020 May;26(5):504-517. doi: 10.1111/cns.13280. Epub 2019 Dec 23.
4
TDP43 pathology in the brain, spinal cord, and dorsal root ganglia of a patient with FOSMN.伴有 FOSMN 的患者大脑、脊髓和背根神经节中的 TDP43 病理学改变。
Neurology. 2019 Feb 26;92(9):e951-e956. doi: 10.1212/WNL.0000000000007008. Epub 2019 Jan 30.
5
Facial Onset Motor and Sensory Neuronopathy Syndrome With a Novel TARDBP Mutation.伴有新型TARDBP突变的面部起病的运动和感觉神经元病综合征
Neurologist. 2019 Jan;24(1):22-25. doi: 10.1097/NRL.0000000000000201.
6
Taste changes in amyotrophic lateral sclerosis and effects on quality of life.肌萎缩侧索硬化症中的味觉变化及其对生活质量的影响。
Neurol Sci. 2019 Feb;40(2):399-404. doi: 10.1007/s10072-018-3672-z. Epub 2018 Dec 4.
7
Neuronal glucose metabolism is impaired while astrocytic TCA cycling is unaffected at symptomatic stages in the hSOD1 mouse model of amyotrophic lateral sclerosis.在肌萎缩侧索硬化症的 hSOD1 小鼠模型的症状阶段，神经元的葡萄糖代谢受损，而星形胶质细胞的 TCA 循环不受影响。
J Cereb Blood Flow Metab. 2019 Sep;39(9):1710-1724. doi: 10.1177/0271678X18764775. Epub 2018 Mar 19.
8
Evolution of the neurochemical profiles in the G93A-SOD1 mouse model of amyotrophic lateral sclerosis.肌萎缩侧索硬化症 G93A-SOD1 小鼠模型中的神经化学特征演变。
J Cereb Blood Flow Metab. 2019 Jul;39(7):1283-1298. doi: 10.1177/0271678X18756499. Epub 2018 Feb 5.
9
Facial Onset Sensory and Motor Neuronopathy: Further Evidence for a TDP-43 Proteinopathy.面部起病的感觉和运动神经元病：TDP-43蛋白病的进一步证据
Case Rep Neurol. 2015 Apr 23;7(1):95-100. doi: 10.1159/000381944. eCollection 2015 Jan-Apr.
10
Facial onset sensory and motor neuronopathy (FOSMN) of childhood onset.儿童期起病的面部起病感觉和运动神经元病（FOSMN）
Muscle Nerve. 2014 Oct;50(4):614-5. doi: 10.1002/mus.24299.