Sickle cell-thalassemia disease



sickle cell-thalassemia disease n.
See microdrepanocytic anemia.

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    noun, Pathology. 1. the usually asymptomatic hereditary condition that occurs when a person inherits from only one parent the abnormal hemoglobin gene characteristic of sickle cell anemia. sickle cell trait n. A hereditary condition, usually harmless and without symptoms, in which an individual carries only one gene for sickle cell anemia.

  • Sickle-feather

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