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Composition and metabolism of myelin, and genetic leukodystrophies Kunihiko Suzuki 1,2 pp.172-181
Published Date 1983/4/10
DOI https://doi.org/10.11477/mf.1431905482
  • Abstract
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 The term, "genetic leukodystrophy", implies an apparent contradiction. "Genetic" indicates uniform presence of the fundamental abnormality throughout the body, while "leukodystrophy"indicates that the clinicopathological manifestations are more or less limited to the central nervous system white matter and the peripheral nerves. This leads to a simplistic generalization. In a genetic leukodystrophy, the fundamental genetic defect must be located in the metabolic pathway of a constituent unique to myelin or its parent cells, the oligodendroglia or Schwann cells.


Copyright © 1983, Igaku-Shoin Ltd. All rights reserved.

基本情報

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

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