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肌张力障碍——左旋多巴反应性还是青少年帕金森病?

Dystonia--L-dopa responsive or juvenile parkinsonism?

作者信息

Rondot P, Ziegler M

出版信息

J Neural Transm Suppl. 1983;19:273-81.

PMID:6583312
Abstract

Four cases of dystonia occurring in two families are reported. The first symptoms consisting of dystonia and rigidity appeared early in childhood, in the first months in one family and of ages two and five years respectively in the other. In two cases, transient tremor was noted. These four children have been treated with L-dopa with prompt spectacular results, in cases 1 and 2, with more gradual less complete results in the others. L-dopa treatment was continued twelve, eleven, six, and five years, respectively, without any developmental problems. Motor function remains satisfactory and school work is normal. The only secondary effect observed was the occurrence of dyskinesia. The relation between L-dopa responsive dystonia and Parkinson's disease is discussed.

摘要

本文报告了两个家族中出现的4例肌张力障碍病例。最初症状为肌张力障碍和僵硬,均在儿童早期出现,其中一个家族在最初几个月出现,另一个家族分别在2岁和5岁时出现。2例出现短暂性震颤。这4名儿童均接受了左旋多巴治疗,病例1和病例2迅速取得显著疗效,其他病例疗效较缓慢且不完全。左旋多巴治疗分别持续了12年、11年、6年和5年,未出现任何发育问题。运动功能保持良好,学业正常。观察到的唯一副作用是出现运动障碍。文中讨论了左旋多巴反应性肌张力障碍与帕金森病之间的关系。

相似文献

1
Dystonia--L-dopa responsive or juvenile parkinsonism?肌张力障碍——左旋多巴反应性还是青少年帕金森病?
J Neural Transm Suppl. 1983;19:273-81.
2
[Dopa-sensitive dystonia].[多巴敏感性肌张力障碍]
Rev Neurol (Paris). 1992;148(11):680-6.
3
Dopa responsive dystonia and juvenile Parkinson's disease: two subtypes of the same disorder?多巴反应性肌张力障碍与青少年帕金森病:同一疾病的两种亚型?
Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):451-4.
4
[Two siblings of juvenile Parkinson's disease dystonic type (Yokochi type 3) and hereditary progressive dystonia with marked diurnal fluctuation (Segawa)].[青少年帕金森病肌张力障碍型(横池3型)和伴有明显昼夜波动的遗传性进行性肌张力障碍(濑川)的两名兄弟姐妹]
Rinsho Shinkeigaku. 1989 Jul;29(7):890-4.
5
[Levodopa and controlled release benserazide in the handling of motor fluctuations in Parkinson's disease].左旋多巴与复方卡比多巴控释片用于治疗帕金森病运动波动
Rev Med Chil. 1991 Sep;119(9):1022-8.
6
Drug-induced motor complications in dopa-responsive dystonia: implications for the pathogenesis of dyskinesias and motor fluctuations.多巴反应性肌张力障碍中的药物诱导运动并发症:对异动症和运动波动发病机制的影响
Clin Neuropharmacol. 1999 Jul-Aug;22(4):216-9.
7
Treatment of Parkinson's disease: levodopa as the first choice.帕金森病的治疗:左旋多巴为首选。
J Neurol. 2002 Sep;249 Suppl 2:II19-24. doi: 10.1007/s00415-002-1204-4.
8
[A new levodopa benserazide preparation for Parkinson's disease with motor fluctuations refractory to standard L-dopa].[一种用于治疗对标准左旋多巴治疗反应不佳且伴有运动波动的帕金森病的新型左旋多巴苄丝肼制剂]
Medicina (B Aires). 1991;51(6):561-7.
9
Patient benefits of l-dopa and a decarboxylase inhibitor in the treatment of Parkinson's disease in elderly patients.左旋多巴和脱羧酶抑制剂治疗老年帕金森病患者的患者获益情况。
Pharmatherapeutica. 1985;4(2):132-40.
10
A family with hereditary juvenile dystonia-parkinsonism.一个患有遗传性青少年肌张力障碍-帕金森综合征的家族。
Mov Disord. 1995 Jul;10(4):482-8. doi: 10.1002/mds.870100413.

引用本文的文献

1
Dopa-responsive dystonia--clinical and genetic heterogeneity.多巴反应性肌张力障碍——临床和遗传异质性。
Nat Rev Neurol. 2015 Jul;11(7):414-24. doi: 10.1038/nrneurol.2015.86. Epub 2015 Jun 23.
2
Childhood dystonias.儿童肌张力障碍
Curr Treat Options Neurol. 2015 Mar;17(3):339. doi: 10.1007/s11940-015-0339-4.
3
Clinical variants of idiopathic torsion dystonia.特发性扭转性肌张力障碍的临床变异型
J Neurol Neurosurg Psychiatry. 1989 Jun;Suppl(Suppl):96-100. doi: 10.1136/jnnp.52.suppl.96.
4
The genetics of primary torsion dystonia.原发性扭转性肌张力障碍的遗传学
Hum Genet. 1990 Jan;84(2):107-15. doi: 10.1007/BF00208922.