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Sep 28, 2000 · Clinical characteristics. Beta-thalassemia (β-thalassemia) has two clinically significant forms, β-thalassemia major and β-thalassemia intermedia, caused by absent or reduced synthesis of the hemoglobin subunit beta (beta globin chain). Individuals with β-thalassemia major present between ages six and 24 months with pallor due to severe ...
Feb 24, 2021 · The clinical significance of the spectrum of interactions of CAP+1 (A→C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
May 31, 2022 · Thalassemia is an inherited blood disorder, which means that it is passed from parents to children through genes . There are two main types of thalassemia: alpha thalassemia and beta thalassemia. Each of these types can be mild, moderate, or serious, depending on how much hemoglobin your body makes.
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.
Dec 11, 2022 · Beta thalassaemia is caused by deletions or mutations of the beta globin gene on chromosome 11. Beta thalassaemia is divided broadly into two groups of diseases depending on the number of genes affected: If one copy of the beta globin gene is affected it is referred to as thalassaemia trait/minor
Feb 9, 2024 · Beta thalassemia is a blood disorder that affects the production of hemoglobin. Hemoglobin is the iron-rich protein in your red blood cells that carries oxygen throughout your body.
Jan 4, 2023 · Beta thalassemia intermedia. This is a moderate form of thalassemia. You may need treatment and blood transfusions, so your body has healthy hemoglobin and red blood cells. Beta thalassemia major ...
