Hutchinson-Gilford Progeria Syndrome (HGPS)
Moumita Ghosh, Amity University Kolkata Introduction Hutchinson-Gilford progeria syndrome (HGPS) is a rare disease that affects 1 in every 4-8 million infants worldwide. It is a disease characterized by accelerated aging in humans. Progeroid syndromes (PSs) can be identified as rare and fatal genetic disorders characterized by various features and symptoms of premature physiological aging. […]