Conditions / Genetic

common variable immunodeficiency 10

info ยท Genetic

A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the NFKB2 gene on chromosome 10q24.

Signs and symptoms

  • Central adrenal insufficiency
  • Abnormal response to ACTH stimulation test
  • Decreased circulating IgG concentration
  • Decreased circulating IgM concentration
  • Asthma
  • Combined immunodeficiency
  • Recurrent viral upper respiratory tract infections
  • Decreased circulating IgA concentration
  • Recurrent pneumonia
  • Recurrent oral herpes