Hutchinson-Gilford Progeria Syndrome
Hutchinson-Gilford Progeria Syndrome (HGPS), commonly referred to as progeria, is a rare genetic condition characterized by accelerated aging in children. This progressive disorder significantly impacts physical development, often leading to severe cardiovascular complications and reduced lifespan. Causes and Genetic Basis HGPS is caused by a mutation in the LMNA gene, responsible for producing the lamin