Hereditary neutrophilia
A rare genetic immune disease characterized by chronic neutrophilia increase in the percentage of circulating CD34+ cells in peripheral blood increase in granulocyte precursors in bone marrow and splenomegaly. Patients are predominantly asymptomatic but may present with systemic inflammatory response syndrome with fever dyspnea tachycardia pleural and pericardial effusion or myelodysplastic syndrome.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Hereditary neutrophilia?
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Advocacy Organizations
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.