Thalassemia and Sickle Cell Anaemia are common genetic disorders, with options for treatment and prevention available.

Iron overload remains a significant challenge in the management of β-thalassemia. Early diagnosis and regular monitoring are ...

and local programs related to thalassemia, including screening and diagnosis, monitoring and surveillance, treatment and care programs, research, and others. The committee will provide guidance on ...

or vitamin B-12 cause symptoms. More severe anemia and hereditary spherocytosis may require blood transfusions to treat. A bone marrow transplant could also be performed. People with thalassemia ...

Over 10,000-15000 new cases of thalassemia are diagnosed in India each year. India, with its vast population, is contributing to approximately 25 per cent of the global beta thalassemia reported ...