The following is a summary of “Assessment of ferritin and hepcidin levels in splenectomised and non-splenectomised ...

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 crucial for preventing organ damage. While chelation therapy is the ...

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 ...

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 ...