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