Sickle cell-hemoglobin C disease syndrome

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Sickle cell-hemoglobin C disease syndrome

Synonyms: HbSC disease

A rare genetic hemoglobinopathy characterized by anemia reticulocytosis and erythrocyte abnormalities including target cells irreversibly sickled cells and crystal-containing cells. Clinical course is similar to sickle cell disease but less severe and with less complications. Signs and symptoms may include acute episodes of pain splenic infarction and splenic sequestration crisis acute chest syndrome focal segmental glomerulosclerosis ischemic brain injury peripheral retinopathy and osteonecrosis.

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 Data version March 2024

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Clinical Trials

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