Kostmann syndrome

Orpha code: 99749OMIM code: 610738

Definicja

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
Klasyfikacja

Disease

Synonimy
Infantile agranulocytosis
Agranulocytoza dziecięca
Ciężka wrodzona neutropenia typu 3
Severe congenital neutropenia type 3
Kod ORPHA
99749
Kod OMIM
610738
Kod ICD10
D70
Kod ICD11
4B00.00

No additional description.

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