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Consideration on two cases of dystonia-parkinsonism.

作者信息

Zambrino C A, Balottin U, Borgatti R, Lanzi G

机构信息

Divisione di Neuropsichiatria Infantile, Fondazion Istituto Neurologico C. Mondino, IRCCS, Università di Pavia.

出版信息

Ital J Neurol Sci. 1991 Oct;12(5):475-8. doi: 10.1007/BF02335509.

DOI:10.1007/BF02335509
PMID:1720114
Abstract

We describe two sporadic cases of dystonia-parkinsonism at different stages of disease progression. The two girls, first seen at the ages of 10 and 12 years, have been followed for 9 and 2 years respectively. In both patients L-dopa 60 mg + carbidopa 6 mg brought about a swift remission of symptoms, which persists to date. All examinations, including CT and MR brainscans, were normal. The CSF and urine levels of HVA and 5HIAA were low in one case and normalized with treatment. This finding might provide a fairly valid predictive index of responsiveness to L-dopa.

摘要

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本文引用的文献

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Dystonia musculorum deformans: implications of therapeutic response to levodopa and carbamazepine.变形性肌张力障碍:左旋多巴和卡马西平治疗反应的意义
Arch Neurol. 1982 Jun;39(6):376-7. doi: 10.1001/archneur.1982.00510180054014.
2
[Description of a case of dystonia musculorum deformans treated with L-dopa].[一例用左旋多巴治疗的变形性肌张力障碍病例描述]
Riv Neurobiol. 1981 Jul-Dec;27(34):584-90.
3
Treatment of non-fluctuating progressive dystonia: a neuropharmacological approach.非波动性进行性肌张力障碍的治疗:一种神经药理学方法。
Neuropediatrics. 1984 Oct;15(4):208-10. doi: 10.1055/s-2008-1052368.
4
Juvenile parkinsonism--some clinical, pharmacological, and neuropathological aspects.青少年帕金森病——一些临床、药理学及神经病理学方面的情况
Adv Neurol. 1984;40:407-13.
5
Idiopathic dystonia-parkinsonism with marked diurnal fluctuation of symptoms.伴有明显症状日波动的特发性肌张力障碍 - 帕金森综合征
Ann Neurol. 1985 Jan;17(1):39-45. doi: 10.1002/ana.410170110.
6
Hereditary dystonia-parkinsonism syndrome of juvenile onset.
Neurology. 1986 Nov;36(11):1424-8. doi: 10.1212/wnl.36.11.1424.
7
DOPA-sensitive progressive dystonia of childhood with fluctuations of symptoms--Segawa's syndrome and possible variants. Results of a collaborative study of the European Federation of Child Neurology Societies (EFCNS).
Neuropediatrics. 1986 May;17(2):81-5. doi: 10.1055/s-2008-1052506.
8
Kinetic study of catecholamine metabolism in hereditary progressive dystonia.遗传性进行性肌张力障碍中儿茶酚胺代谢的动力学研究
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Adv Neurol. 1976;14:215-33.