FOLLOW US ON INSTAGRAM!  PRF's Mission is to discover treatments & the cure for Hutchinson-Gilford Progeria Syndrome & its aging-related disorders, including heart disease.

FOLLOW US ON INSTAGRAM! PRF's Mission is to discover treatments & the cure for Hutchinson-Gilford Progeria Syndrome & its aging-related disorders, including heart disease.

This is a condition known as Hutchinson-Gilford Progeria Syndrome. It is a very rare condition that accelerates the aging process in children. The average life span for children with this disorder is 13 years of age.

This is a condition known as Hutchinson-Gilford Progeria Syndrome. It is a very rare condition that accelerates the aging process in children. The average life span for children with this disorder is 13 years of age.

Rupesh Kumar, from Hanumanganj, India, has the body of a 160-year-old. His condition, known as Hutchinson-Gilford progeria, affects just one in eight million people and is incurable.

A 21-year-old man has the body of a 160-year-old

Rupesh Kumar, from Hanumanganj, India, has the body of a 160-year-old. His condition, known as Hutchinson-Gilford progeria, affects just one in eight million people and is incurable.

Progeria (also known as “Hutchinson–Gilford progeria syndrome” and “Hutchinson–Gilford syndrome”) is an extremely rare, severe, genetic condition wherein symptoms resembling aspects of aging are manifested at an early age.

Progeria (also known as “Hutchinson–Gilford progeria syndrome” and “Hutchinson–Gilford syndrome”) is an extremely rare, severe, genetic condition wherein symptoms resembling aspects of aging are manifested at an early age.

"This weekend, in a heartbreaking phone call from his parents, I learned of the death of Sam Berns, a courageous young man with Hutchinson-Gilford Progeria Syndrome. Sam may have only lived 17 years, but in his short life he taught the rest of us a lot about how to live." - NIH Director Francis Collins on 1/12/2013. Photo of Collins with cookie monster and Sam Berns at TEDMED 2012

"This weekend, in a heartbreaking phone call from his parents, I learned of the death of Sam Berns, a courageous young man with Hutchinson-Gilford Progeria Syndrome. Sam may have only lived 17 years, but in his short life he taught the rest of us a lot about how to live." - NIH Director Francis Collins on 1/12/2013. Photo of Collins with cookie monster and Sam Berns at TEDMED 2012

Hayley Okines, who suffered from an extremely rare genetic condition called Hutchinson Gilford Progeria Syndrome, died April 3rd.  She was 17 yrs old.

Hayley Okines, who suffered from an extremely rare genetic condition called Hutchinson Gilford Progeria Syndrome, died April 3rd. She was 17 yrs old.

Hutchinson-Gilford Progeria Syndrome: This syndrome is caused by mutations in the LMNA gene that result in the production of an abnormal version of the lamin A protein. The altered protein makes the nuclear envelope unstable and progressively damages the nucleus, making cells more likely to die prematurely. The disease causes premature aging and severe hardening of the arteries beginning in childhood. This condition greatly increases the chances having a heart attack or stroke at a young…

Hutchinson-Gilford Progeria Syndrome: This syndrome is caused by mutations in the LMNA gene that result in the production of an abnormal version of the lamin A protein. The altered protein makes the nuclear envelope unstable and progressively damages the nucleus, making cells more likely to die prematurely. The disease causes premature aging and severe hardening of the arteries beginning in childhood. This condition greatly increases the chances having a heart attack or stroke at a young…

Hutchinson-Gilford Progeria Syndrome or Accelerated Aging. Super Duper sad.

10 Weird Health Problems

Hutchinson-Gilford Progeria Syndrome or Accelerated Aging. Super Duper sad.

Pinterest
Search