Literature DB >> 3694233

Neuropathological changes of the brain in myotonic dystrophy--some new observations.

S Ono1, K Inoue, T Mannen, F Kanda, K Jinnai, K Takahashi.   

Abstract

Brain autopsy materials from 2 patients with myotonic dystrophy (MyD) were studied. The results obtained in these 2 cases were quite similar. Besides thalamic inclusion bodies and minor abnormalities in gyral architecture with a disordered cortical cellular arrangement, some new observations have been made. First, no more than one intracytoplasmic inclusion body per cell was present in the cerebral cortex, the thalamus, the caudate nucleus and the putamen; this inclusion body was oval or elongated with smooth, sharply defined contours and was usually located at the periphery of the cell. Second, irregular intracytoplasmic inclusion bodies, often multiple and not surrounded by a halo, were found at the periphery or within accumulations of neuromelanin granules in the pigmented cells of the substantia nigra. All the bodies described above stained highly eosinophilic with hematoxylin-eosin and the ultrastructure of the bodies in the thalamus and the substantia nigra was almost the same; these bodies were composed of stacks of alternating parallel, light and dark rectilinear profiles oriented perpendicularly to the longitudinal axis of the bodies. Third, Marinesco bodies were observed with a very high frequency in the pigmented cells of the substantia nigra.

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Mesh:

Year:  1987        PMID: 3694233     DOI: 10.1016/0022-510x(87)90105-5

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  13 in total

1.  Novel eosinophilic inclusion in astrocytes.

Authors:  H Abe; S Yagishita; K Itoh; S Hamano
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

2.  Cerebral and muscle MRI abnormalities in myotonic dystrophy.

Authors:  Daniel T Franc; Ryan L Muetzel; Paul R Robinson; Craig P Rodriguez; Joline C Dalton; Cameron E Naughton; Bryon A Mueller; Jeffrey R Wozniak; Kelvin O Lim; John W Day
Journal:  Neuromuscul Disord       Date:  2012-01-30       Impact factor: 4.296

3.  Intracytoplasmic inclusion bodies of the thalamus and the substantia nigra, and Marinesco bodies in myotonic dystrophy: a quantitative morphological study.

Authors:  S Ono; K Inoue; T Mannen; S Mitake; T Shirai; F Kanda; K Jinnai; K Takahashi
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

4.  Intracytoplasmic eosinophilic inclusions in the neurons of the central nervous system.

Authors:  C E Peña; A Katoh
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

5.  Apathy and hypersomnia are common features of myotonic dystrophy.

Authors:  J S Rubinsztein; D C Rubinsztein; S Goodburn; A J Holland
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-04       Impact factor: 10.154

6.  Neuropsychological profile in myotonic dystrophy.

Authors:  B Censori; M Danni; M Del Pesce; L Provinciali
Journal:  J Neurol       Date:  1990-07       Impact factor: 4.849

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Journal:  J Biol Chem       Date:  2011-12-19       Impact factor: 5.157

8.  White matter abnormalities and neurocognitive correlates in children and adolescents with myotonic dystrophy type 1: a diffusion tensor imaging study.

Authors:  Jeffrey R Wozniak; Bryon A Mueller; Erin E Ward; Kelvin O Lim; John W Day
Journal:  Neuromuscul Disord       Date:  2010-12-18       Impact factor: 4.296

9.  Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia.

Authors:  Marla Gearing; Jorge L Juncos; Vincent Procaccio; Claire-Anne Gutekunst; Elaine M Marino-Rodriguez; Kymberly A Gyure; Shoichiro Ono; Robert Santoianni; Nicolas S Krawiecki; Douglas C Wallace; Bruce H Wainer
Journal:  Ann Neurol       Date:  2002-10       Impact factor: 10.422

10.  Structural disorder and the loss of RNA homeostasis in aging and neurodegenerative disease.

Authors:  Douglas A Gray; John Woulfe
Journal:  Front Genet       Date:  2013-08-14       Impact factor: 4.599

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