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Sickle cell-thalassemia disease: anemia clinically resembling sickle cell anemia, in which those affected are compound heterozygous for the sickle cell gene and a thalassemia gene; about 60-80% of hemoglobin is Hb S, up to 20% Hb F, and the remainder Hb A. SYN: microdrepanocytic anemia.
Source: Stedman's Medical Spellchecker, © 2006 Lippincott Williams & Wilkins. All rights reserved.
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Source: Diseases Database
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