Literature DB >> 8482990

Follow-up of neurophysiological tests and CT in late-onset cerebellar ataxia and multiple system atrophy.

K Wessel1, G P Huss, H Brückmann, D Kömpf.   

Abstract

The follow-up of neurophysiological tests (brain-stem auditory evoked potentials; blink reflex; sensory, motor and visual evoked potentials) and CT was investigated in 21 patients with late-onset cerebellar ataxia (CA) or multiple system atrophy. The study included an initial investigation and a follow-up examination on average 25.3 months later (minimum 8, maximum 36). Patients were divided into four groups: (1) those with pure CA after a minimum course of 5 years; (2) those with pure CA with pathological neurophysiological findings at the last examination; (3) those who at the first examination clinically presented with pure CA, but at the last examination were seen to have developed a multisystem disorder; (4) those with multiple system atrophy (mostly olivopontocerebellar atrophy) presenting additional non-cerebellar signs of involvement. Conforming to a strict interpretation of pure CA, group 1 patients invariably exhibited normal neurophysiological findings at all examinations. All patients in group 4, except for 2 only at the first examination, showed pathological changes in at least one of the neurophysiological tests. The main conclusion of this paper is that individuals who according to clinical criteria were initially classified as having CA but finally developed a multisystem disorder already had pathological neurophysiological findings at the initial examination (group 3). The increasing frequency of pathology in the several neurophysiological tests together with the progression of the disease is obviously of prognostic significance. CT revealed cerebellar atrophy without apparent involvement of brain-stem structures in all patients with CA; the majority of patients with multiple system atrophy also had atrophy of the brain-stem, pointing to olivopontocerebellar atrophy.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Year:  1993        PMID: 8482990     DOI: 10.1007/bf00857523

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  24 in total

Review 1.  The olivopontocerebellar atrophies: a review.

Authors:  B W Konigsmark; L P Weiner
Journal:  Medicine (Baltimore)       Date:  1970-05       Impact factor: 1.889

2.  Visual, auditory and somatosensory pathway involvement in hereditary cerebellar ataxia, Friedreich's ataxia and familial spastic paraplegia.

Authors:  L Pedersen; W Trojaborg
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1981-10

3.  [Early auditory evoked potentials in spinocerebellar heredodegenerative involvement].

Authors:  A Belkahia; M Ben H'mida; N Ben Jelloul; A Gassab; A Chakroun
Journal:  Ann Otolaryngol Chir Cervicofac       Date:  1985

4.  Olivopontocerebellar atrophy. A review of 117 cases.

Authors:  J Berciano
Journal:  J Neurol Sci       Date:  1982-02       Impact factor: 3.181

5.  The development of infratentorial atrophy in patients with idiopathic cerebellar ataxia of late onset: a CT study.

Authors:  T Klockgether; J Faiss; M Poremba; J Dichgans
Journal:  J Neurol       Date:  1990-11       Impact factor: 4.849

6.  Cerebellar atrophy: the differential diagnosis by computerized tomography.

Authors:  S L Rothman; S Glanz
Journal:  Neuroradiology       Date:  1978       Impact factor: 2.804

7.  Computed tomography of olivopontocerebellar degeneration.

Authors:  M Savoiardo; M Bracchi; A Passerini; A Visciani; S Di Donato; F Cocchini
Journal:  AJNR Am J Neuroradiol       Date:  1983 May-Jun       Impact factor: 3.825

8.  Evoked potentials in olivopontocerebellar atrophy.

Authors:  E J Hammond; B J Wilder
Journal:  Arch Neurol       Date:  1983-06

9.  Correlation of clinical signs with CT findings in patients with cerebellar disease.

Authors:  H C Diener; A Müller; A Thron; M Poremba; J Dichgans; H Rapp
Journal:  J Neurol       Date:  1986-02       Impact factor: 4.849

10.  Brainstem auditory evoked responses in spinocerebellar degeneration and Wilson disease.

Authors:  M Fujita; M Hosoki; M Miyazaki
Journal:  Ann Neurol       Date:  1981-01       Impact factor: 10.422

View more
  1 in total

1.  Sporadic adult onset ataxia of unknown etiology : a clinical, electrophysiological and imaging study.

Authors:  M Abele; M Minnerop; H Urbach; K Specht; T Klockgether
Journal:  J Neurol       Date:  2007-10-15       Impact factor: 4.849

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.