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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.
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 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 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.
Thalassemia major is the most severe form
of
beta
thalassemia.
It develops when
beta globin genes are missing.
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Far far away, behind the word mountains, far from the countries Vokalia and Consonantia
Far far away, behind the word mountains, far from the countries Vokalia and Consonantia
Far far away, behind the word mountains, far from the countries Vokalia and Consonantia