Conditions / Genetic
agammaglobulinemia 8A
info · Genetic
An agammaglobulinemia that has_material_basis_in heterozygous dominant-negative mutation in the TCF3 gene on chromosome 19p13.
Signs and symptoms
- Agammaglobulinemia
- Recurrent infections
- Decreased total B cell count
- Recurrent otitis media
- Post-vaccination polio