The Karnataka government has accorded administrative approval to implement a universal newborn screening scheme for congenital and metabolic disorders in the Kalyana Karnataka region. The scheme, to be implemented at a cost of ₹5.58 crore, aims to screen newborns for five metabolic disorders — hypothyroidism, congenital adrenal hyperplasia, galactosemia, phenylketonuria, and glucose-6-phosphate dehydrogenase deficiency (G6PD deficiency).

The scheme will cover seven districts — Bidar, Kalaburagi, Yadgir, Raichur, Koppal, Ballari, and Vijayanagar — excluding mining-affected areas.

The government has directed authorities to conduct surveys in healthcare institutions across these districts to identify shortages of medical equipment required for detecting rare metabolic disorders and to procure them within the sanctioned grant limits.

Healthcare personnel are to be trained in conducting newborn screening and related procedures, according to the order. The government's move is expected to improve healthcare services for newborns in the region, with the next steps involving the implementation of the scheme and training of healthcare personnel.