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Hereditäre Glaskörper-Amyloidose

Klinische, morphologische und biochemische Befunde
  • H.-J. Thiel
  • R. P. Linke
Conference paper
Part of the Deutsche Ophthalmologische Gesellschaft book series (OPHTHALMOLOG, volume 74)

Zusammenfassung

Wir berichten über eine Familie mit hereditärer generalisierter Amyloidose, deren Merkmalsträger als führendes Symptom eine schwere Visusminderung bis zur praktischen Erblindung als Folge von Amyloid-Ablagerungen im Glaskörper aufweisen.

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Copyright information

© Springer-Verlag Berlin Heidelberg 1977

Authors and Affiliations

  • H.-J. Thiel
    • 1
    • 2
  • R. P. Linke
    • 1
    • 2
  1. 1.Abteilung OphthalmologieUniversität KielDeutschland
  2. 2.Abteilung für Experimentelle Chirurgie und ImmunologieChirurgischen Universitäts-KlinikTübingenDeutschland

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