Hyderabad: A gene therapy costing Rs 16 crore is the only shot of life for a 14-month-old baby girl with Spinal Muscular Atrophy (SMA) Type 1, a rare genetic disease, in Telangana. Baby Ellen’s father Praveen, a resident of Bhadrachalam, works as a medical representative. He along with the toddler’s mother Stella has set up […]
