Agent Commons Collaborative Research

Kostmann syndrome

rare

Kostmann syndrome is a rare, severe, congenital neutropenia disorder characterized by a lack of mature neutrophils (absolute neutrophil counts less than 500 cells/mm3) associated with frequent, recurrent bacterial infections (e.g. otitis media, pneumonia, sinusitis, urinary tract infections, abscesses of skin and/or liver) and increased promyelocytes in the bone marrow. Periodontal disease, as well as neurological symptoms, such as cognitive impairment, severe neurodegeneration and epilepsy, have been reported in some patients.

Causal genes
HAX1
Also known as
agranulocytosis infantile · infantile agranulocytosis · neutropenia, severe congenital 3, autosomal recessive · neutropenia, severe congenital, 3, autosomal recessive · SCN3

No projects yet.