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Progeria, the "Aging Disease"

Laymen have called it the “aging disease,” but the correct medical term is Hutchinson-Gilford Progeria Syndrome. The medical community generally refers to it as progeria. The word Progeria comes from the Greek progeros, meaning 'prematurely old'. Progeria is a rare, progressive, genetic disorder causing children to age rapidly.

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August 28, 2013: Hutchinson-Gilford Progeria Syndrome is an extremely rare genetic disease wherein symptoms resembling aspects of aging are manifested at a very early age. The word progeria comes from the Greek words "pro" (πρό), meaning "before" or "premature", and "gēras" (γῆρας), meaning "old age". The disorder has a very low incident rate, occurring in an estimated 1 per 8 million live births.

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Hutchinson-Gilford Progeria Roughly one in four million newborns suffer from Progeria, which is a genetic condition that causes rapid aging. As babies, they maintain a normal appearance, but as they grow older, they develop bulging eyes, protruding ears, small chins, thin noses and poor skin. Their arteries harden, increasing their chances of enduring a heart attack or stroke. People with Progeria typically live until their early-teens, though some can live until the age of 30.

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from io9

10 Unusual Genetic Mutations in Humans

Progeria This genetic disorder is as rare as it is severe. The classic form of the disease, called Hutchinson-Gilford Progeria, causes accelerated aging.

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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

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Hutchinson-Gilford Progeria Syndrome.png

Promising treatment for Progeria within reach ~ Sahlgrenska Academy, University of Gothenburg, Sweden. Progeria is a rare genetic childhood disorder characterized by the appearance of accelerated aging. The classical form of progeria, called Hutchinson-Gilford Progeria Syndrome (HGPS), is caused by a spontaneous mutation, which means that it is not inherited from the parents. Children with HGPS usually die in their teenage years from myocardial infarction and stroke.

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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.

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Hayley Okines suffers from an extremely rare genetic condition called Hutchinson Gilford Progeria Syndrome, also known as HGPS or Progeria.

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