Describe thalasemia in brief...
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Thalasemia
it is the genetic disorder which occurs in humen
Thalassemia is an autosomal, inherited
recessive disease. Haemoglobin molecule is
made of four polypeptide chains- 2 alpha (a)
and 2 beta (b) chains. The synthesis of alpha
chains are controlled by two closely linked
genes (HBA1 and HBA2) on chromosome
16 while the synthesis of beta chain is controlled
by a single gene (HBB) on chromosome
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Thalassemia is an inherited blood disorder in which the body makes an abnormal form of hemoglobin. Hemoglobin is the protein molecule in red blood cells that carries oxygen. The disorder results in excessive destruction of red blood cells, which leads to anemia.
Symptoms: Anemia
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