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Biochemische Untersuchungsergebnisse bei Morbus Fabry

  • Conference paper
Achtzigster Kongress

Part of the book series: Verhandlungen der Deutschen Gesellschaft für Innere Medizin ((VDGINNERE,volume 80))

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Zusammenfassung

Das Angiokeratoma corporis diffusum, der Morbus Fabry, ist eine erbliche Glykolipidstoffwechselerkrankung mit X-chromosomal geschlechtsgebundenem Erbgang. Die Erkrankung ist charakterisiert durch die systematische Anhäufung eines Glykosphingolipids, eines Ceramid-Trihexosids [1] (Abb. 1), in zahlreichen Geweben.

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Literatur

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Authors and Affiliations

  1. II. Med. Klinik u Poliklinik Univ. Mainz, Deutschland

    W. Atzpodien, G. J. Kremer, E. Schnellbacher & H. Bierbach

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  1. W. Atzpodien
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  2. G. J. Kremer
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  3. E. Schnellbacher
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  4. H. Bierbach
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© 1974 Springer-Verlag Berlin Heidelberg

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Atzpodien, W., Kremer, G.J., Schnellbacher, E., Bierbach, H. (1974). Biochemische Untersuchungsergebnisse bei Morbus Fabry. In: Achtzigster Kongress. Verhandlungen der Deutschen Gesellschaft für Innere Medizin, vol 80. J.F. Bergmann-Verlag, Munich. https://doi.org/10.1007/978-3-642-85449-1_372

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  • DOI: https://doi.org/10.1007/978-3-642-85449-1_372

  • Publisher Name: J.F. Bergmann-Verlag, Munich

  • Print ISBN: 978-3-8070-0293-4

  • Online ISBN: 978-3-642-85449-1

  • eBook Packages: Springer Book Archive

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