Chuvash erythrocytosis
Name: |
Chuvash erythrocytosis
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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.
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ORPHAcode: |
238557
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Synonyms: |
Chuvash polycythemia
Von Hippel-Lindau-dependent polycythemia
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
22 Jun 2023 - 16:14
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