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Nov 14, 2019 · The disorder results in excessive destruction of red blood cells, which leads to anemia. Anemia is a condition in which your body doesn’t have enough normal, healthy red blood cells. Thalassemia...
Jun 3, 2022 · 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.
Symptoms depend on the type of thalassemia and can vary from none to severe. [1] Often there is mild to severe anemia (low red blood cells or hemoglobin) as thalassemia can affect the production of red blood cells and also affect how long the red blood cells live. [1]
Aug 31, 2022 · Thalassemia is a genetic blood disorder that impacts the ability of the blood to get oxygen to the body’s organs. Learn about the signs, how it’s diagnosed & treated. Skip to main content
May 31, 2022 · Thalassemia is an inherited blood disorder that causes the body to make fewer healthy red blood cells and less hemoglobin than normal. Learn more about the causes, symptoms, and treatment for the condition.
May 15, 2024 · 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.
Jul 20, 2022 · Beta thalassemia is one of two main types of thalassemia. Beta thalassemia and its counterpart, alpha thalassemia, involve gene mutations (or errors) in the hemoglobin protein. This gene mutation disrupts your body’s ability to make a protein in hemoglobin called beta-globin.
Thalassemias are a group of inherited microcytic, hemolytic anemias characterized by defective hemoglobin synthesis. Alpha-thalassemia is particularly common among people with African, Mediterranean, or Southeast Asian ancestry. Beta-thalassemia is more common among people with Mediterranean, Middle Eastern, Southeast Asian, or Indian ancestry.
Thalassemia is an inherited (i.e., passed from parents to children through genes) blood disorder caused when the body doesn’t make enough of a protein called hemoglobin, an important part of red blood cells.
May 15, 2024 · Treatments for thalassemia depend on the type and how serious it is. Blood transfusions are the main way to treat moderate or severe thalassemia. People receiving regular blood transfusions are at risk for certain complications such as iron overload, alloimmunization (a harmful immune reaction), and infection.
