India, Nov. 13 -- For a nine-month-old child, the road ahead should be measured in first words, first steps and the small discoveries of infancy. But for the daughter of a Delhi University faculty member, the immediate concern is a rare genetic disorder and a treatment bill running into crores. Now, in a significant gesture of institutional support, the university has approved Rs 17 crore in financial assistance for her treatment.

The decision follows months of efforts by colleagues, teachers and well-wishers who came together to raise money for the child's medical care. Diagnosed with Spinal Muscular Atrophy (SMA) Type-II, a rare genetic disorder affecting muscle strength and movement, the infant requires specialised treatment at an age...