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What is Thalassemia?

Thalassemia is a genetically inherited blood disorder which directly affects the production of haemoglobin protein. Haemoglobin is a very essential protein that is required by the body to have a healthy production of red blood cells. In patients who suffer from various kinds of thalassemia, the red blood cells will be less in production and the ones produced will not complete its complete life cycle.

Most of the common symptoms are:

  1. Fatigue
  2. Weakness
  3. Pale or yellow skin tone
  4. Delayed growth
  5. Bone deformities
  6. Dark urine

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What is Thalassaemia ?

Thalassemia is a
genetic blood disorder that causes hemoglobin deficiency
and severe anemia, starving organs of oxygen, which inhibits their ability to function properly.

Alpha Thalassemia

Alpha thalassemia is a blood disorder that reduces the production of hemoglobin . Hemoglobin is the protein in red blood cells that carries oxygen to cells throughout the body.

Beta Thalassemia

Beta thalassemia is a blood disorder that reduces the production of hemoglobin. Hemoglobin is the iron-containing protein in red blood cells that carries oxygen to cells throughout the body.

Most
Severe Type of
Thalassaemia

Thalassemia major is the most severe form
of
beta
thalassemia.
It develops when
beta globin genes are missing.





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