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Muskeldystrophien, Myotonien und metabolische Myopathien Bearbeitet

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Klinische Neurologie

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Zusammenfassung

Muskeldystrophien bilden eine klinisch und genetisch heterogene Gruppe primär degenerativer, progressiver Muskelerkrankungen. Das Manifestationsalter reicht von der frühen Kindheit bis in das mittlere und späte Erwachsenenalter. Bei vielen Formen ist inzwischen der zugrundeliegende Genort, bei einigen Formen auch das defekte Genprodukt bekannt. Dies hat zu einer neuen Klassifikation der Muskeldystrophien geführt.

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Authors
  1. K. Eger
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  2. W. J. Schulte-Mattler
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  3. K. Hertel
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  4. M. Deschauer
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  5. A. Lindner
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  6. S. Zierz
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Editor information

Editors and Affiliations

  1. Klinik für Neurologie mit Klinischer Neurophysiologie, Alfried-Krupp-Krankenhaus, Alfried-Krupp-Straße 21, D-45131, Essen, Deutschland

    Peter Berlit

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© 1999 Springer-Verlag Berlin Heidelberg

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Eger, K., Schulte-Mattler, W.J., Hertel, K., Deschauer, M., Lindner, A., Zierz, S. (1999). Muskeldystrophien, Myotonien und metabolische Myopathien Bearbeitet. In: Berlit, P. (eds) Klinische Neurologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-08118-1_10

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  • DOI: https://doi.org/10.1007/978-3-662-08118-1_10

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-08119-8

  • Online ISBN: 978-3-662-08118-1

  • eBook Packages: Springer Book Archive

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