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sickle cell C disease

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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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The American Heritage® Stedman's Medical Dictionary Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.

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