Pediatric Thalassemia

Pediatric thalassemia is a genetic blood disorder where the body produces an abnormal form or insufficient amount of hemoglobin, the protein that carries oxygen in red blood cells. This leads to anemia, causing fatigue, weakness, and delayed growth in affected children. Depending on severity, children may require regular blood transfusions and iron chelation therapy to prevent complications. Thalassemia is inherited, meaning a child gets the gene from their parents. While it’s a lifelong condition, proper medical care can help manage symptoms and improve quality of life. Early diagnosis and treatment are essential for better health outcomes.