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. to clinically asymptomatic individuals.
What is Thalassemia?
· may cause a person to feel tired, weak or short of breath. This is a condition called anemia. People with thalassemia may have mild or severe anemia. Severe anemia can damage organs and lead to death. What are the different types of thalassemia?
Thalassemia: MedlinePlus Medical Encyclopedia
· Thalassemia minor occurs if you receive the faulty gene from only one parent. People with this form of the disorder are carriers of the disease. Most of the time, they do not have symptoms. Beta thalassemia major is also called Cooley anemia. Risk factors for
Beta Thalassemia (for Parents)
· Beta thalassemia is an inherited blood disorder in which the body doesn’t make hemoglobin normally. Hemoglobin is the part of red blood cells (RBCs) that carries oxygen throughout the body. The abnormal hemoglobin can lead to anemia (not enough RBCs …
Testing for Thalassemia Trait
Thalassemia carriers have smaller red blood cells that may cause a mild anemia. The anemia is so mild that it does not require medical treatment. Trait carriers should not take iron supplements unless a special blood test (serum iron or serum ferritin) shows that you are iron deficient.
Anemia (also spelled anaemia) is a decrease in the total amount of red blood cells (RBCs) or hemoglobin in the blood, or a lowered ability of the blood to carry oxygen. When anemia comes on slowly, the symptoms are often vague and may include feeling tired, weakness, shortness of breath, and a poor ability to exercise.
· Alpha-thalassemia is a blood disorder that reduces the body’s production of hemoglobin.Affected people have anemia, which can cause pale skin, weakness, fatigue, and more serious complications.Two types of alpha-thalassemia can cause health problems: the
Alpha Thalassemia Types, Diagnosis, and Treatment
· Alpha thalassemia is an inherited condition and requires both parents to be carriers. A person without alpha thalassemia should have four alpha globin genes. The risk of having a child with alpha thalassemia disease is dependent on the status of the parents. The trans form of alpha thalassemia minor is more common in people of African descent.
Paleness: Causes, Symptoms, Diagnosis, and Treatment
· Anemia is a condition in which your body doesn’t produce enough red blood cells. It’s one of the most common causes of paleness. Anemia can be acute with a …
Beta Thalassemia Clinical Presentation: History and …
· 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 thalassemia (ie, thalassemia major) causes severe, transfusion-dependent anemia.