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