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An autopsied case of familial sudanophilic leukodystrophy, with reference to its autopsied cousin case having thalamus degeneration Nobumasa KATO 1 , Shinsaku OYANAGI 2 , Toshiaki ABE 3 , Masaaki MATSUSHITA 4 , Hiromoto YASUDA 5 , Koichi HANADA 1 , Hajime KAZAMATSURI 1 , Masaya ODA 6 1Department of Psychiatry, School of Medicine, Teikyo University 2Division of Ultrastructure and Histochemistry, Psychiatric Research Institute of Tokyo 3Department of Pediatrics, School of Medicine, Teikyo University 4Division of Neuropathology, Psychiatric Research Institute of Tokyo 5Department of Pathology, School of Medicine, Teikyo University 6Department of Neuropathology, Brain Research Institute, Faculty of Medicine, University of Tokyo pp.330-339
Published Date 1980/4/10
DOI https://doi.org/10.11477/mf.1431905164
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Abstract

27-year-old female, with progressive mental deterioration and neurological symptoms, was autopsied and the neuropathological examinations confirmed that she had had sudanophilic leuko-dystrophy. The family from which she stemmed have yielded may patients with neurological or mental disorders in recent successive generations (Fig. 1), and one of her cousin had thalamus degeneration which was confirmed neuropatholo-gically by Oda et al. in 1965 (5). One of her elder sister, 33 years old at present, is now under medical care and observation showing similar symptoms to the patient.


Copyright © 1980, 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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