Conditions / Genetic

common variable immunodeficiency 3

info ยท Genetic

A common variable immunodeficiency that has_material_basis_in homozygous or compound heterozygous mutation in the CD19 gene on chromosome 16p11.2.

Signs and symptoms

  • Decreased class-switched memory B cell proportion
  • Combined immunodeficiency
  • Chronic decreased circulating total IgG concentration
  • Decreased circulating isohemagglutinin concentration
  • Recurrent otitis media
  • Decreased circulating IgM concentration
  • Decreased circulating IgA concentration
  • Recurrent sinusitis
  • Recurrent bacterial infections
  • Recurrent respiratory infections