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A rare cause of elevated chitotriosidase activity: Glycogen storage disease type iv

  • Hacettepe University
  • Intergen Genetics Center

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

6 Citations (Scopus)

Abstract

Human chitinolytic enzyme named “chitotriosidase” takes part in the defense mechanism against pathogens and the homeostasis of innate immunity. Chitotriosidase was firstly reported to be markedly high in plasma of patients with Gaucher disease. Abnormal lipid laden macrophages are thought to be responsible for stimulating the secretion of chitotriosidase in Gaucher disease. Subsequently, various disorders have also been found to be associated with elevated levels of chitotriosidase. Chronic liver diseases that are also related with macrophage activation may have elevated chitotriosidase activity. We report the second case of the literature with glycogen storage disease (GSD) type IV that presented with high chitotriosidase levels. GSD type IV should be taken into consideration in case of elevated chitotriosidase levels, stigmas of chronic liver disease, and inconsistency of lysosomal storage diseases.

Original languageEnglish
Title of host publicationJIMD Reports
PublisherSpringer
Pages63-66
Number of pages4
DOIs
Publication statusPublished - 2014

Publication series

NameJIMD Reports
Volume17
ISSN (Print)2192-8304
ISSN (Electronic)2192-8312

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Gauche disease
  • Glycogen storage disease
  • Glycogen storage disease type
  • Lysosomal storage disease
  • Metachromatic leukodystrophy

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