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Japanese

Evaluation of Cranial CT Findings of Patients with Muscular Dystrophy:With a Reference to Cerebral Vascular Disease and Cardiac Complications Masaaki Konagaya 1 , Motoko Sakai 1 , Satoshi Kuru 1 , Takashi Kato 1 , Fumihiko Yasuma 2 , Yukihiko Matsuoka 1 1Department of Neurology, Suzuka National Hospital 2Department of Internal Medicine, Suzuka National Hospital Keyword: muscular dystrophy , stroke , brain atrophy , cerebral embolism , dilated cardiomyopathy pp.621-626
Published Date 1999/7/1
DOI https://doi.org/10.11477/mf.1406901464
  • Abstract
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We evaluated cranial CT findings of 160 patients with various type of progressive muscular dystrophy (PMD). Significant brain atrophy was observed in 21 out of 63 cases of Duchenne muscular dystrophy (DMD), 7 out of 15 Becker muscular dystrophy (BMD), no case of 2 female dytrophinopathy (F-dyst), 11 out of 21 limb-girdle muscular dystrophy (LG) , all cases of 10 Fukuyama type congenital mus-cular dystrophy (FCMD), 2 out of 5 fascioscapulohu-meral muscular dystrophy (FSH), and 32 out of 44 myotonic dystrophy (MyD). Genetical degenerative process and vascular insufficiency seemed to causebrain atrophy in these disease.


Copyright © 1999, Igaku-Shoin Ltd. All rights reserved.

基本情報

電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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