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Sialic Acids pp 307–320Cite as

Sialidoses

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Part of the book series: Cell Biology Monographs ((CELLBIOL,volume 10))

Abstract

The term sialidosis has been introduced recently to denote a group of patients with an inherited defect in the catabolism of sialic acid-containing oligosaccharides and glycoproteins. Sialidosis, therefore, belongs to the category of the so-called oligosaccharidoses (Maroteaux and Humbel 1976), metabolic diseases which are characterized by an excessive accumulation of glycoprotein-derived oligosaccharides.

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Authors and Affiliations

  1. Department of Pathochemistry, University of Heidelberg, Heidelberg, Federal Republic of Germany

    Michael Cantz

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  1. Michael Cantz
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Editors and Affiliations

  1. Biochemisches Institut, Christian-Albrechts-Universität, Kiel, Federal Republic of Germany

    Roland Schauer

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Cantz, M. (1982). Sialidoses. In: Schauer, R. (eds) Sialic Acids. Cell Biology Monographs, vol 10. Springer, Vienna. https://doi.org/10.1007/978-3-7091-8680-0_11

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  • DOI: https://doi.org/10.1007/978-3-7091-8680-0_11

  • Publisher Name: Springer, Vienna

  • Print ISBN: 978-3-7091-8682-4

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