Search results
Jul 20, 2022 · 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.
Beta thalassemias (β thalassemias) are a group of inherited blood disorders. They are forms of thalassemia caused by reduced or absent synthesis of the beta chains of hemoglobin that result in variable outcomes ranging from severe anemia to clinically asymptomatic individuals. Global annual incidence is estimated at one in 100,000. [4] .
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 ...
May 1, 2023 · Beta-thalassemia refers to an inherited mutation of the beta-globin gene, causing a reduced beta-globin chain of hemoglobin. The highest prevalence of beta-thalassemia mutations is in people of Mediterranean, Middle Eastern, and Asian descent.
Dec 6, 2023 · Beta-thalassaemia is an inherited blood disorder caused by mutations of the beta-globin gene that results in ineffective erythropoiesis. Spectrum of severity from asymptomatic to severe anaemia and skeletal changes.
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.
Jan 26, 2024 · Beta thalassemia syndromes are a group of hereditary disorders characterized by a genetic deficiency in the synthesis of beta-globin chains. In the homozygous state, beta...
