Get Thalassemia Mediterranean Anemia PNG. Mediterranean anemia, also called thalassemia, is a blood disorder inherited from defective genes in one or both parents. Those afflicted have less hemoglobin and fewer red blood cells than normal.
Thalassemia (Mediterranean anemia): Symptoms, Causes ... from asset21.ckassets.com Thalassemia is an inherited blood disorder. Mediterranean anemia, also called thalassemia, is a blood disorder inherited from defective genes in one or both parents. Thalassemia , group of blood disorders characterized by a deficiency of hemoglobin , the blood protein that.
Alpha thalassemia is a blood disorder in which the body has a problem producing alpha globin, a component of hemoglobin, the protein in red blood cells that transports oxygen throughout the body.
Beta thalassemia major causes hemolytic anemia, poor growth, and skeletal abnormalities during infancy. Thalassemias are a heterogeneous group of hereditary blood disorders characterized by faulty globin chain synthesis resulting in defective hemoglobin, which can lead to anemia. Symptoms depend on the type and can vary from none to severe. This condition is marked by a lack of oxygen being.
