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拉姆齐-亨特综合征中正常的肌肉线粒体功能

Normal muscle mitochondrial function in Ramsay-Hunt syndrome.

作者信息

Sacquegna T, Montagna P, Moggio M, De Carolis P, Agati R, Bresolin N

机构信息

Istituto di Clinica Neurologica, Università di Bologna.

出版信息

Ital J Neurol Sci. 1989 Feb;10(1):73-5. doi: 10.1007/BF02333875.

DOI:10.1007/BF02333875
PMID:2925347
Abstract

Mitochondrial encephalomyopathies may display clinical features similar to Ramsay-Hunt syndrome (RHS). We studied muscles mitochondrial function in 2 patients with RHS. Histochemical and ultrastructural studies of muscle biopsies and biochemical analysis of muscle mitochondrial enzymes were normal. There is no evidence for a disturbance of muscle mitochondrial function in RHS.

摘要

线粒体脑肌病可能表现出与拉姆齐-亨特综合征（RHS）相似的临床特征。我们研究了2例RHS患者的肌肉线粒体功能。肌肉活检的组织化学和超微结构研究以及肌肉线粒体酶的生化分析均正常。没有证据表明RHS存在肌肉线粒体功能障碍。

相似文献

1
Normal muscle mitochondrial function in Ramsay-Hunt syndrome.拉姆齐-亨特综合征中正常的肌肉线粒体功能
Ital J Neurol Sci. 1989 Feb;10(1):73-5. doi: 10.1007/BF02333875.
2
Dyssynergia cerebellaris myoclonica (Ramsay Hunt syndrome): a condition unrelated to mitochondrial encephalomyopathies.肌阵挛性小脑协同失调（拉姆齐·亨特综合征）：一种与线粒体脑肌病无关的病症。
J Neurol Neurosurg Psychiatry. 1989 Feb;52(2):262-5. doi: 10.1136/jnnp.52.2.262.
3
Mitochondrial myopathy and lactic acidaemia with myoclonic epilepsy, ataxia and hypothalamic infertility: a variant of Ramsay-Hunt syndrome?伴有肌阵挛性癫痫、共济失调和下丘脑性不育的线粒体肌病和乳酸性血症：拉姆齐-亨特综合征的一种变异型？
J Neurol Neurosurg Psychiatry. 1981 Jan;44(1):79-82. doi: 10.1136/jnnp.44.1.79.
4
The Ramsay Hunt syndrome revisited: Mediterranean myoclonus versus mitochondrial encephalomyopathy with ragged-red fibers and Baltic myoclonus.再探拉姆齐·亨特综合征：地中海肌阵挛与伴有破碎红纤维的线粒体脑肌病及波罗的海肌阵挛
Acta Neurol Scand. 1990 Jan;81(1):8-15. doi: 10.1111/j.1600-0404.1990.tb00924.x.
5
Ramsay Hunt syndrome in dentatorubral-pallidoluysian atrophy.
Pediatr Neurol. 1985 Sep-Oct;1(5):298-301. doi: 10.1016/0887-8994(85)90032-3.
6
[Myoclonic cerebellar dyssynergia (Ramsay-Hunt syndrome) and cerebellar telangiectasia].肌阵挛性小脑协同失调（拉姆齐-亨特综合征）与小脑毛细血管扩张症
Rev Neurol (Paris). 1986;142(1):29-33.
7
[Myoclonic cerebellar dyssynergia (Ramsay Hunt syndrome)].
Med Clin (Barc). 1986 Jan 18;86(2):78-82.
8
[Familial olivo-ponto-cerebellar atrophy with myoclonus. Limits of cerebellar myoclonic dyssynergia (Ramsay-Hunt syndrome)].[伴有肌阵挛的家族性橄榄体脑桥小脑萎缩。小脑性肌阵挛性协同失调（拉姆齐-亨特综合征）的局限]
Rev Neurol (Paris). 1976 Feb;132(2):113-24.
9
[Electroencephalographic study of myoclonic cerebellar dyssynergia with epilepsy (Ramsay-Hunt syndrome)].
Rev Electroencephalogr Neurophysiol Clin. 1974 Jul-Sep;4(3):407-28. doi: 10.1016/s0370-4475(74)80052-3.
10
[A case of dyssynergia cerebellaris myoclonica (Ramsay-Hunt syndrome)].
Neurologija. 1983;31(1-2):63-74.

本文引用的文献

1
Mitochondrial myopathy and lactic acidaemia with myoclonic epilepsy, ataxia and hypothalamic infertility: a variant of Ramsay-Hunt syndrome?伴有肌阵挛性癫痫、共济失调和下丘脑性不育的线粒体肌病和乳酸性血症：拉姆齐-亨特综合征的一种变异型？
J Neurol Neurosurg Psychiatry. 1981 Jan;44(1):79-82. doi: 10.1136/jnnp.44.1.79.
2
Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature.伴有破碎红纤维（线粒体异常）的肌阵挛性癫痫：疾病实体还是综合征？两例病例的光镜和电镜研究及文献复习
J Neurol Sci. 1980 Jul;47(1):117-33. doi: 10.1016/0022-510x(80)90031-3.
3
[Myoclonic cerebellar dyssynergy (Ramsay Hunt syndrome)].
肌阵挛性小脑协同失调（拉姆齐·亨特综合征）
Rev Neurol (Paris). 1968 Jul;119(1):85-106.
4
[Electroencephalographic study of myoclonic cerebellar dyssynergia with epilepsy (Ramsay-Hunt syndrome)].
Rev Electroencephalogr Neurophysiol Clin. 1974 Jul-Sep;4(3):407-28. doi: 10.1016/s0370-4475(74)80052-3.
5
The clinical features of mitochondrial myopathy.线粒体肌病的临床特征。
Brain. 1986 Oct;109 ( Pt 5):915-38. doi: 10.1093/brain/109.5.915.
6
The syndrome of myoclonic epilepsy with ragged-red fibers. Report of a case and review of the literature.伴有破碎红纤维的肌阵挛性癫痫综合征。病例报告及文献复习。
Neuropediatrics. 1987 Nov;18(4):200-4. doi: 10.1055/s-2008-1052480.
7
Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle.致命性婴儿细胞色素c氧化酶缺乏症：肌肉中免疫可检测酶的减少。
Neurology. 1985 Jun;35(6):802-12. doi: 10.1212/wnl.35.6.802.