An 8-year-old boy, wheelchair-bound due to a rare genetic disease, HPDL deficiency, regained his mobility through an experimental drug, 4-HB. This groundbreaking treatment, bypassing the CoQ10 deficiency, restored his ability to walk and engage in activities like hiking and go-karting. Post navigation GSEB HSC Result 2025: Gujarat class 12th science supplementary results declared Kanwar Yatra: ‘Sanatani’ stickers on Delhi shops; VHP certifies vegetarian-only outlets
