Sickle cell c disease



sickle cell C disease n.
A hereditary blood disease caused by sickle-shaped red blood cells that contain hemoglobin S and hemoglobin C, characterized by anemia, blocked blood vessels, chronic leg ulcers, and bone deformities.

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  • Sickle cell disease

    sickle cell disease n. See sickle cell anemia.

  • Sickle cell hemoglobin

    sickle cell hemoglobin n. See hemoglobin S.



  • Sickle cell retinopathy

    sickle cell retinopathy n. A condition characterized by dilation and tortuosity of retinal veins, microaneurysms, and retinal hemorrhages, with advanced cases manifesting neovascularization, detachment of the retina, or vitreous hemorrhage.

  • Sickle cell syndrome

    sickle cell syndrome n. See sickle cell anemia.



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