Conditions / Genetic

common variable immunodeficiency 11

info ยท Genetic

A common variable immunodeficiency that has_material_basis_in homozygous mutation in the IL21 gene on chromosome 4q27.

Signs and symptoms

  • Inflammation of the large intestine
  • Increased circulating IgE concentration
  • Crohn's disease
  • Decreased class-switched memory B cell proportion
  • Fatigue
  • Failure to thrive
  • Clubbing of fingers
  • Mucoid diarrhea
  • Aphthous ulcer
  • Recurrent respiratory infections