Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition 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. Disease data Classification Disease Synonyms Infantile agranulocytosis Agranulocytoza dziecięca Ciężka wrodzona neutropenia typu 3 Severe congenital neutropenia type 3 ORPHA code 99749 OMIM code 610738 ICD10 code D70 ICD11 code 4B00.00 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl