Inflammatory bowel disease in glycogen storage disease type Ib

J Pediatr. 1986 Jul;109(1):55-9. doi: 10.1016/s0022-3476(86)80572-8.

Abstract

We have observed the development of chronic inflammatory bowel disease, indistinguishable from Crohn disease, in two boys with glycogen storage disease type Ib (GSD-Ib). A chance association of these diseases in two patients is unlikely. Studies of their neutrophils showed severe chronic neutropenia (mean absolute granulocyte counts of less than 500 cells/microliter) and markedly deficient chemotactic response (less than 5% of reference values) in the patients with GSD-Ib and normal neutrophil values in four patients with glycogen storage disease type Ia (GSD-Ia). Monocyte counts and responses to chemotactic stimulation were normal in both GSD-Ia and GSD-Ib. Chronic inflammatory bowel disease appears to be associated with GSD-Ib, and neutrophil abnormalities may be involved in the pathogenesis of the bowel inflammation.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Chemotaxis, Leukocyte
  • Child
  • Child, Preschool
  • Crohn Disease / complications*
  • Crohn Disease / immunology
  • Crohn Disease / metabolism
  • Glycogen Storage Disease Type I / complications*
  • Glycogen Storage Disease Type I / immunology
  • Glycogen Storage Disease Type I / metabolism
  • Glycogen Storage Disease Type I / physiopathology
  • Humans
  • Infant
  • Leukocyte Count
  • Monocytes / physiology
  • Neutrophils / physiology