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Sialic Acids pp 307-320 | Cite as

Sialidoses

  • Michael Cantz
Part of the Cell Biology Monographs book series (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.

Keywords

Sialic Acid Mild Form Lysosomal Storage Disease Galactosidase Activity Lysosomal Hydrolase 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag/Wien 1982

Authors and Affiliations

  • Michael Cantz
    • 1
  1. 1.Department of PathochemistryUniversity of HeidelbergHeidelbergFederal Republic of Germany

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