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