Literature DB >> 1895148

Brain stem atrophy in Joseph disease: a morphometric study using two-dimensional (area) measurement by computed tomography.

Y Fukutani1, K Katsukawa, Y Ishizaki, K Kobayashi, I Nakamura.   

Abstract

Eight Japanese patients with Joseph disease were studied using computed tomography (CT). Morphometric analysis using the two-dimensional (area) measurement by CT was performed in the infratentorial region. The brain-stem index, an index of brain-stem atrophy or pontine atrophy, revealed a significant decrease (P less than 0.01), with a mean of 66.7% when compared with 16 control subjects. The patients showed a significant increase (P less than 0.01), with a mean of three times that of the controls in the fourth ventricular index, an index of fourth ventricular dilatation. There were no differences in the cerebellar index, an index of cerebellar atrophy, between these patients and the controls, although the patients had an increased number of visible cerebellar vermian (2.0, SD 0.7) and hemispheric sulci (2.6 SD 0.6) as compared with the controls (vermian sulci: 0.4, SD 0.7: hemispheric sulci: 0). These data indicate severe pontine atrophy, fourth ventricular dilatation with mild involvement of the cerebellum and correlate well with the common pathological features of Joseph disease. The present morphometric evaluation by CT may be useful in the clinical diagnosis of Joseph disease.

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Year:  1991        PMID: 1895148     DOI: 10.1007/bf00314778

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


  17 in total

1.  [Peculiar forms of familial olivo-ponto-cerebellar atrophy (Menzel type) and Joseph disease; clinico-neuropathological study of two families with nosological considerations].

Authors:  T Ikeda
Journal:  Seishin Shinkeigaku Zasshi       Date:  1987

2.  Machado disease. A hereditary ataxia in Portuguese emigrants to Massachusetts.

Authors:  K K Nakano; D M Dawson; A Spence
Journal:  Neurology       Date:  1972-01       Impact factor: 9.910

3.  Joseph's disease: clinical and pathological studies in a Japanese family.

Authors:  T Yuasa; E Ohama; H Harayama; M Yamada; Y Kawase; M Wakabayashi; T Atsumi; T Miyatake
Journal:  Ann Neurol       Date:  1986-02       Impact factor: 10.422

4.  CT findings in spinocerebellar degeneration.

Authors:  A Ramos; F Quintana; C Díez; C Leno; J Berciano
Journal:  AJNR Am J Neuroradiol       Date:  1987 Jul-Aug       Impact factor: 3.825

5.  [Computed tomography in spinocerebellar degenerations (author's transl)].

Authors:  H Yamamoto; M Konagaya; N Murakami; T Takayanagi; I Sobue
Journal:  Rinsho Shinkeigaku       Date:  1980-07

6.  Joseph disease in a non-Portuguese family.

Authors:  T Sakai; M Ohta; H Ishino
Journal:  Neurology       Date:  1983-01       Impact factor: 9.910

7.  Clinical criteria for diagnosis of Machado-Joseph disease: report of a non-Azorena Portuguese family.

Authors:  L Lima; P Coutinho
Journal:  Neurology       Date:  1980-03       Impact factor: 9.910

8.  Presumably Azorean disease in a presumably non-Portuguese family.

Authors:  E B Healton; J C Brust; D L Kerr; S Resor; A Penn
Journal:  Neurology       Date:  1980-10       Impact factor: 9.910

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.  Computerized tomography in hereditary ataxias.

Authors:  L Pedersen; C Gyldensted
Journal:  Acta Neurol Scand       Date:  1978-08       Impact factor: 3.209

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  1 in total

1.  Delirium associated with Joseph disease.

Authors:  Y Fukutani; K Katsukawa; R Matsubara; K Kobayashi; I Nakamura; N Yamaguchi
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-11       Impact factor: 10.154

  1 in total

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