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Japanese

Congenital spinocerebellar degeneration associated with atrophy of brain stern tegmentum and sensory nucleus Kazuro TAKAHASHI 1 , Haruomi NAKAMURA 1 , Masataka ARIMA 2 , Toshio NAKASHIMA 3 1Division of Neuropathology, Tottori University School of Medicine 2Childhood Neurology, Tottori University School of Medicine 3National Sanatorium Matsue Hospital pp.107-114
Published Date 1974/2/10
DOI https://doi.org/10.11477/mf.1431903605
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An autopsy case of congenital spinocerebellar degeneration with an autosonal recessive inherity was reported. He was a 15 years old boy, whosesister had the same symptomes and the parentswere cousins. He had severe dementia, myoclonus and rigospastic contructure. On pathological study, sever degenerations were found in the cerebellum, namely, the mollecular and granular layer and dentatorubral system. The number of Purkinje cells were reduced, moderately. In the pons, the tegmentum was severely atrophied and the pons nucleus were normal.


Copyright © 1974, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1243 印刷版ISSN 0001-8724 医学書院

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