Imerslund-Gräsbeck syndrome in a Saudi family

Acta Paediatr Scand. 1991 Nov;80(11):1109-12. doi: 10.1111/j.1651-2227.1991.tb11795.x.

Abstract

Imerslund-Gräsbeck syndrome, an autosomal recessive trait of defective uptake of intrinsic factor-vitamin B12 complex by terminal ileum, is described in a Saudi family (two siblings and their first cousin). This rare disease has previously been reported only in Northern Europe and North African Jewish ethnic groups.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Anemia, Megaloblastic / epidemiology
  • Anemia, Megaloblastic / genetics*
  • Child
  • Humans
  • Male
  • Pedigree
  • Saudi Arabia
  • Syndrome
  • Vitamin B 12 / metabolism
  • Vitamin B 12 Deficiency / epidemiology
  • Vitamin B 12 Deficiency / genetics*

Substances

  • Vitamin B 12