Progeria, also known as Hutchinson-Gilford Progeria Syndrome (HGPS), is a rare genetic disorder characterized by rapid aging in children. It is a progressive condition that affects various aspects of a child's development and overall health.
Synonyms for Progeria:
Progeria is caused by a mutation in the LMNA gene, which leads to the production of an abnormal protein called progerin. This protein affects the structure and function of the cell nucleus, resulting in the characteristic signs and symptoms of Progeria.
Children with Progeria typically exhibit growth failure, loss of body fat and hair, joint stiffness, cardiovascular problems, and a higher susceptibility to various diseases. Despite these challenges, individuals with Progeria often possess normal intelligence and a vibrant personality.
While there is currently no cure for Progeria, ongoing research aims to better understand the condition and develop potential treatments. Supportive care, including regular monitoring of cardiovascular health and physical therapy, can help manage the symptoms and improve the quality of life for individuals with Progeria.