Chuvash erythrocytosis

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Name:
Chuvash erythrocytosis
Description:
Chuvash erythrocytosis is a rare, genetic, congenital secondary polycythemia disorder characterized by increased hemoglobin, hematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnea and/or plethora. Patients present an increased risk of hemorrhage, thrombosis and early death.
ORPHAcode:
238557
Synonyms:
Chuvash polycythemia
Von Hippel-Lindau-dependent polycythemia
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14