Biology, asked by Anonymous, 9 months ago

Describe thalasemia in brief...

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Answered by Anonymous

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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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Answered by Anonymous

Answer:

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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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