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单词 thalassemia
释义 thalassemia
 /thal'euh see"mee euh/, n. Pathol.
 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. Also called Cooley's anemia.
 [1932; < Gk thálass(a) sea (alluding to the Mediterranean Sea; the anemia was first reported among children in Mediterranean countries) + -EMIA]
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