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Progeria | Hutchinson–Gilford Progeria Syndrome (HGPS)

Hutchinson–Gilford Progeria Syndrome (HGPS)

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Introduction… | Progeria

https://progeriaproject.wordpress.com/2010/11/17/introduction

Progeria, also known as Hutchinson-Guilford Progeria Syndrome (HGPS) is an extremely rare genetic condition wherein symptoms resembling extreme rapid ageing are evident at an early age. For every one year of natural life, those with Progeria age between 5-7 years. As terribly sad as this disease is, i find it absolutely fascinating how the human body can age so rapidly and i really wanted to find out more about it. Soon after this there was a series of documentaries on Channel 4 in England called ‘...

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1.What is Progeria? | Progeria

https://progeriaproject.wordpress.com/what-is-progeria

HGPS is a very rare genetic disorder. Characteristic facies, wrinkled skin, prominent scalp veins, typical posture and gait, sculpted nose , and stunted growth will lead to the diagnosis. Normal motor and mental development. No demonstrable abnormalities of growth hormone, thyroid stimulating hormone, parathyroid hormone, and adrenal hormones. Presence of abnormal collagen. Varying degrees of generalised atherosclerosis involving chiefly the larger arteries in post-mortem studies. Currently, there are le...

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3.Case Studies | Progeria

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A six-year-old white girl was first seen at a hearing and speech clinic in rural Missouri. The childs mother brought her to the clinic seeking recommendations for special education facilities because. The child seemed “quite fragile” She was referred to a Medical Centre, Kansas City, Missouri,for evaluation, and diagnosis because of her obviously abnormal appearance. The skull appeared grossly abnormal with prominence of the frontal regions. The ears were prominent and low set. The lungs and heart and ab...

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5.Development for a cure? | Progeria

https://progeriaproject.wordpress.com/development-for-a-cure

5Development for a cure? While there might not yet be an actual cure for the prevention of Progeria; there are several drugs and medical procedures that can help reduce the effects of the condition. There is a drug known as Nifedipine. In August 2005 and February 2006, researchers published studies that support a potential drug treatment for children with Progeria. Farnesyltransferase inhibitors (FTIs). In May 2007, the first ever Progeria Clinical Drug Trial began with the Progeria Research Foundation.

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4.Children living with Progeria | Progeria

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4Children living with Progeria. Researching information on children with Progeria and watching videos and seeing pictures was incredibly sad to do. It really moved me to see how brave these little children were, and how absolutely gorgeous and happy they were, despite knowing how different they are. I tried to find videos that give a true reflection of how these children actually feel and how they deal with living with Progeria. Tragically though, Ashley passed away just one month before her 18th birthda...

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Progeria Pictures | Photos of Hutchinson-Gilford Syndrome

Progeria, also knowns as Hutchinson-Gilford Syndrome, is a genetic condition that causes its victims to age prematurely. Although it is rare, the idea has surfaced in many pieces of literature and films in popular culture. That Cool Guy says:. Hey guys these progeria jokes are getting old fast. I am the same person as Cool guy says:. Everyone is saying may jesus bless you. What if they are muzzlem. All these people are at least still alive. but that is bc i let them live. Chuck Norris Fan says:. Is surel...

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Progeria: Premature aging

The disease that kills before life begins. Http:/ www.progeriaresearch.org/about progeria.html). Progeria is a sickening disease that quickly ages children, from very early on. Symptoms of Progeria begin before the child even reaches his or her first birthday. Although Progeria affects the entire world, the Caucasian culture experience Progeria. Of ten. By deforming the cells’ basic structure,. Http:/ www.progeria.be/informatie EN.php)-2nd picture. In the age range of 13-20,. What is Progeria exactly?

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Progeria | Hutchinson–Gilford Progeria Syndrome (HGPS)

Progeria, also known as Hutchinson-Guilford Progeria Syndrome (HGPS) is an extremely rare genetic condition wherein symptoms resembling extreme rapid ageing are evident at an early age. For every one year of natural life, those with Progeria age between 5-7 years. As terribly sad as this disease is, i find it absolutely fascinating how the human body can age so rapidly and i really wanted to find out more about it. Soon after this there was a series of documentaries on Channel 4 in England called ‘...

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The Progeria Research Foundation | Together we WILL find the cure!®

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