Thalassemia
noun, Pathology.
1.
a hereditary form of anemia, occurring chiefly in people of Mediterranean origin, marked by the abnormal synthesis of hemoglobin and a consequent shortened life span of red blood cells.
thalassemia thal·as·se·mi·a (thāl’ə-sē’mē-ə)
n.
Any of a group of inherited forms of anemia occurring chiefly among people of Mediterranean descent, caused by faulty synthesis of part of the hemoglobin molecule.
thalassemia
(thāl’ə-sē’mē-ə)
Any of a group of inherited forms of anemia occurring chiefly among people of Mediterranean descent, caused by faulty synthesis of part of the hemoglobin molecule
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