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Mediterranean anaemia

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Noun1.Mediterranean anaemia - an inherited form of anemia caused by faulty synthesis of hemoglobin
monogenic disease, monogenic disorder - an inherited disease controlled by a single pair of genes
hypochromic anaemia, hypochromic anemia - anemia characterized by a decrease in the concentration of corpuscular hemoglobin
Cooley's anaemia, Cooley's anemia, thalassaemia major, thalassemia major - a fatal form of homozygous thalassemia (inherited from both parents) in which there is no hemoglobin; skeletal deformations; heart and spleen and liver enlarged


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Thalassaemia Sometimes called Mediterranean anaemia, Thalassaemia is a genetic disorder that may have originated more than 50,000 years ago in a valley south of Italy and Greece now covered by the Mediterranean.
 
 
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