Thalassemia is one of the most common genetic disorders in the world. It causes anemia because red blood cells are more fragile than normal. Detecting the disease or carrying the gene is important to prevent the risk of severe disease in future generations.

Thalassemia is a congenital hemolytic disease, inherited in a recessive gene pattern on the autosomal chromosome from parents to children through generations. The main manifestation of the disease is anemia with dangerous complications, affecting the race and ethnicity. Performing premarital tests is extremely necessary to accurately screen for Thalassemia genes, helping to determine whether couples carry the Thalassemia gene or not, thereby assessing the risk of Thalassemia in future children.

Hemoglobin electrophoresis is a blood test to detect normal or abnormal Hemoglobin components and their concentrations. Accordingly, hemoglobin electrophoresis is used as a first-line test to approach suspected cases of Hemoglobin, Thalassemia...

Thalassemia is an autosomal recessive genetic disease in which the genes are passed from parents to their children. The disease can be detected early through prenatal genetic testing, screening, and diagnosis.

Thalassemia is a dangerous disease that leaves many complications for the patient as well as a burden on the family. The disease can be prevented by screening, diagnosis through tests and genetic diagnosis.

Hemoglobin is a protein in red blood cells that carries oxygen from the lungs to the rest of the body. There are different types of hemoglobin in red blood cells. Hemoglobin electrophoresis is a test that measures these types of hemoglobin in the blood and looks for abnormal types of hemoglobin, which plays a role in screening and diagnosing thalassemia.

Thalassemia (congenital hemolytic anemia) is a hereditary hemolytic anemia. The disease can leave serious sequelae and become a burden for the family and society. However, the symptoms of the disease can be controlled by maintaining a reasonable diet and rest.