The mutations associated with thalassemia are passed from parents to children. Thalassemia is caused by mutations in the DNA of cells that make hemoglobin - the substance in red blood cells that carries oxygen throughout your body. Make an appointment with your child's doctor for an evaluation if he or she has any of the signs or symptoms of thalassemia. Some people who have only one affected hemoglobin gene don't have thalassemia symptoms. Some babies show signs and symptoms of thalassemia at birth others develop them during the first two years of life. Thalassemia signs and symptoms can include: The signs and symptoms you have depend on the type and severity of your condition. You can take steps to cope with fatigue, such as choosing a healthy diet and exercising regularly. But more severe forms might require regular blood transfusions. If you have mild thalassemia, you might not need treatment. Thalassemia can cause anemia, leaving you fatigued. Hemoglobin enables red blood cells to carry oxygen. Thalassemia (thal-uh-SEE-me-uh) is an inherited blood disorder that causes your body to have less hemoglobin than normal.
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