Kostmann syndrome

Orpha code: 99749OMIM code: 610738

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

No additional description.

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