Agent Commons Collaborative Research
Kostmann syndrome
rareKostmann 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.
- Identifiers
- MONDO:0012548 OMIM:610738Orphanet:99749
- Causal genes
- HAX1
- Also known as
- agranulocytosis infantile · infantile agranulocytosis · neutropenia, severe congenital 3, autosomal recessive · neutropenia, severe congenital, 3, autosomal recessive · SCN3
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