what is beta thalassemia|Beta thalassemia : Clark Beta Thalassemia is a hereditary blood disorder characterized by reduced production of beta-globin chains, which are essential components of hemoglobin. The condition leads to an imbalance in the production of hemoglobin, resulting in anemia and various complications.
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what is beta thalassemia,
Beta thalassemia is an inherited blood disorder that limits your body’s ability to make beta-globin. Beta-globin is an important protein needed to make hemoglobin and red blood cells. Beta thalassemia can cause you to experience anemia symptoms. Types include beta thalassemia major, beta thalassemia intermedia and beta thalassemia minor.
Key points about beta thalassemia. Thalassemia is an inherited blood disorder. It causes the body to make less hemoglobin. There are several types of beta thalassemia. Different people will have different symptoms, based on which type of beta thalassemia is inherited. Treatment of beta thalassemia may include medicines and regular blood .what is beta thalassemiaKey points about beta thalassemia. Thalassemia is an inherited blood disorder. It causes the body to make less hemoglobin. There are several types of beta thalassemia. Different people will have different symptoms, based on which type of beta thalassemia is inherited. Treatment of beta thalassemia may include medicines and regular blood .
Beta-thalassemia is a blood disorder that reduces the body's production of hemoglobin. Low levels of hemoglobin lead to a shortage of mature red blood cells and a lack of oxygen in the body. People with Beta-thalassemia have anemia, which can cause paleness, weakness, fatigue, and more serious complications.Thalassemia is a blood disorder that affects your body’s ability to produce hemoglobin and healthy red blood cells. Types include alpha and beta thalassemia.Beta-thalassemia (β-thalassemia) is an inherited blood disorder, and a form of thalassemia resulting in variable outcomes ranging from clinically asymptomatic to severe anemia individuals. It is caused by reduced or absent synthesis of the beta chains of hemoglobin, the molecule that carries oxygen in the blood. [5] .Beta Thalassemia is a hereditary blood disorder characterized by reduced production of beta-globin chains, which are essential components of hemoglobin. The condition leads to an imbalance in the production of hemoglobin, resulting in anemia and various complications. Beta thalassemia is a treatable blood disorder that’s inherited, or passed down through your genes. With beta thalassemia, your body doesn’t make enough hemoglobin, which is an. When thalassemia is called "alpha" or "beta," this refers to the part of hemoglobin that isn't being made. If either the alpha or beta part is not made, there aren't enough building blocks to make normal amounts of hemoglobin. Low alpha is called alpha thalassemia. Low beta is called beta thalassemia.
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. In people with beta thalassemia, low levels of hemoglobin reduce oxygen levels in the body.
what is beta thalassemia|Beta thalassemia
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