• Meera.S
• Anuja.V.Gopal
• Ashwin Shibu
• Prasobh G R
• Grace N Raju

Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disease that leads premature aging .Progeria cases occur in 1 per four million live births. Because of accelerated aging, a child in ten year will have similar condition that of 70-year old would have. Many children with progeria appear normal at birth and then progressively develop the characteristic features during early childhood. Various methods for diagnosis are being developed and clinical trials on some drugs that may be used in treatment are being done. The goal of this study was to determine sign and symptoms, cause of HGPS and how to treat the occasional illness of progeria.

Keywords: Progeria, sign and symptom, pathophysiology, treatment.

"A REVIEW ON HUTCHINSON GILFORD PROGERIA SYNDROME", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.9, Issue 5, page no.h382-h394, May-2022, Available :http://www.jetir.org/papers/JETIR2205849.pdf

"A REVIEW ON HUTCHINSON GILFORD PROGERIA SYNDROME", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.9, Issue 5, page no. pph382-h394, May-2022, Available at : http://www.jetir.org/papers/JETIR2205849.pdf