A recent study conducted by researchers at the Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, has highlighted the presence of inherited iron metabolism defects among anaemic patients in India. The findings underscore the importance of active screening and awareness campaigns to identify and manage these rare diseases effectively within the population.

Lead researcher Amita Trehan emphasized the significance of this research in addressing the burden of rare inherited defects in the country. “It is crucial to devise strategies for identifying at-risk populations and offering timely interventions such as novel therapeutics or stem cell transplants,” Trehan stated.

While iron deficiency remains the primary cause of anaemia globally, the study reveals the existence of other forms of anaemia related to vitamin deficiencies and sickle cell disease. The call for enhanced screening aims to improve diagnostic capabilities and provide targeted healthcare interventions for affected individuals across India.

As efforts intensify to combat anaemia and related disorders, heightened awareness and proactive screening measures are pivotal in addressing the diverse health needs of the population and advancing public health initiatives.