Beta Thalassemia Major is a severe form of thalassemia, a genetic blood disorder that results in the production of abnormal hemoglobin. This leads to severe anemia, as the red blood cells cannot carry oxygen properly. Symptoms include fatigue, weakness, pale skin, delayed growth, and bone deformities. Individuals with Beta Thalassemia Major often require regular blood transfusions to manage their condition. Over time, iron buildup from these transfusions can lead to complications, requiring chelation therapy. Early diagnosis through blood tests and ongoing medical care are essential for managing the condition and improving quality of life.
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