期刊文献+

针药并用辨证论治遗传性共济失调1例 被引量:3

Acupuncture combined with Medicine and Treatment based on Syndrome Differentiation for Hereditary Ataxia for One Case
下载PDF
导出
摘要 目的观察运用中医辨证论治通过针灸中药联合应用对遗传性共济失调疾病的治疗效果。方法我科采用针刺、电针、灸法、口服中药以补肾益气为法,西医以对症处理为辅治疗。结果经过半年治疗患者症状较前明显改善,治疗效果显著。结论运用中医针药治疗遗传性共济失调可减轻症状,延缓病情发展,能够获得较好疗效。 Objective To observe the therapeutic effect of the combination of acupuncture and moxibustion and Chinese medicine in the treatment of hereditary ataxia. Methods The acupuncture,electro acupuncture,moxibustion,oral administration of traditional Chinese medicine of supplementing qi to tonify the kidney was the method,and the Western medicine mainly symptomatic treatment as auxiliary treatment. Results After six months of treatment,the symptoms of the patients were significantly improved,and the therapeutic effect was significant. Conclusion The use of acupuncture and Chinese medicine in the treatment of hereditary ataxia can relieve symptoms,delay the development of disease,and can get better curative effect.
出处 《光明中医》 2016年第15期2257-2258,共2页 GUANGMING JOURNAL OF CHINESE MEDICINE
关键词 遗传性共济失调 中药 针灸 辨证论治 Hereditary ataxia Traditional Chinese medicine Acupuncture and moxibustion Treatment based on syndrome differentiation
  • 相关文献

参考文献9

二级参考文献65

  • 1谢秋幼,梁秀龄,李洵桦.脊髓小脑性共济失调的分子遗传学诊断与临床应用[J].中华医学遗传学杂志,2005,22(1):71-73. 被引量:13
  • 2李洵桦,梁秀龄,刘焯霖,潘锡榜,胡学强,张成,周钰倩,陈嵘,张影如,潘贺葵,欧翠华,卢锡林.957例神经遗传病分析[J].中华医学遗传学杂志,1994,11(6):372-374. 被引量:33
  • 3Matilla-Duenas A, Sanchez I, Con'al-Juan M, et al. Cellular and molecular pathways triggering neurodegeneration in the spi- nocerebellar ataxias[ J ]. Cerebellum, 2010,9 (2) : 148-166.
  • 4Yoshida K, Shindzu Y, Morita H, et al. Severity and progres- sion rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of Japan [ J ]. Cerebellum, 2009,8 ( 1 ) :46-51.
  • 5Harding A E. Classification of the hereditary ataxias and para- plegias[J]. Lancet, 1983,1(8334) :1151-1155.
  • 6Maruyama H, Kawakami H, Nakamura S. Reevaluation of the exact CAG repeat length in hereditary cerebellar ataxias using highly denaturing conditions and long PCR [ J ]. Hum Genet, 1996,97 (5) :591-595.
  • 7Basri R, Yabe I, Soma H, et al. Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan : a study of 113 Japanese tamilies[ J ]. J Hum Genet, 2007,52(10) :848-855.
  • 8van Swieten J C, Brusse E, de Graaf BM, et al. A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [ corrected] [ J]. Am J Hum Genet, 2003,72( 1 ) :191-199.
  • 9Schols L, Amoiridis G, Buttner T, et al. Autosomal dominant eerebellar ataxia: phenotypic differences in genetically defined subtypes[J] .9 Ann Neurol, 1997,42(6) :924-932.
  • 10Fujigasaki H, Verma I C, Camuzat A, et al. SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family[ J]. Ann Neurol, 2001,49 (1) : 117-121.

共引文献63

同被引文献88

引证文献3

二级引证文献27

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