Though Thalassemia and Sickle Cell Anemia are seemingly similar to the unknowing, a large difference remains; Thalassemia is characterized by a reduced production from one of the globin chains which make up hemoglobin while in Sickle Cell Anemia, the globin chains themselves are structurally defective.
Thalassaemia is not associated with sickle cells in a blood film. However it is categorised similarly, sickle cell anaemia and thalassaemia are both haemoglobinopathies (ie. both are the result of a genetic abnormality of haemoglobin). They can both also be classed as haemolytic anaemias (anaemia due to increased red cell destruction.)
Sickle cell trait can not lead to sickle cell disease. This is because the gene for Red blood cells are dominate over the gene for sickle cell. There for if you have sickle cell you can have some minor symptoms but usually you don't even know you have sickle cell trait. Sickle cell trait is rarely harmful and can almost never turn into sickle cell disease.
Hereditary
Hematologic
Thalassemia is a genetic disorder as a result of an imbalance in the hemoglobin. In sickle cell, also a genetic disorder, the mutation cause a crescent shaped molecule.
Thalassemia is a quantitative problem of too few globins synthesized, whereas sickle-cell anemia (a hemoglobinopathy) is a qualitative problem of synthesis of an incorrectly functioning globin. (wikipedia)
Thalassemia and sickle cell anemia.
If you have beta thalassemia trait and your partner has sickle cell trait there is a 25% chance of your child having sickle beta thalassemia.
Examples: anemia, hemophilia, sickle-cell disease, leukemia, thalassemia, etc.
its optional hemophilia or sickle cell anaemia
Sickle cell anemia and thalassemia are two diseases caused by mutation of the protein hemoglobin.
hemophilia is the deficiency of blood and anemia is the deficiency of red blood cells
i was told many years ago that i couldn't donate as I'm a beta thalassemia carrier. best to ask your local donation center.
The test is used primarily to diagnose diseases involving these abnormal forms of hemoglobin, such as sickle cell anemia and thalassemia.
While technically there are more than one, the main one by far is sickle cell anemia.
many conditions. few include thalassemia, acute blood loss, sickle cell anemia, vitamin B12 or folic acid or iron deficiency, post infection anemia, hereditary spherocytosis.