Taking a Look at Progeria

Hutchinson-Gilford Progeria Syndrome other wise known as “Progeria”, or “HGPS”, is a very rare, and fatal genetic disorder characterized by an appearance of accelerated aging in young children. The rate of aging is accelerated up to seven times that of a normal life span in first 13 years of life. Progeria comes from the Greek word (πρό), “pro” meaning premature and (γῆρας), “gerias” meaning old age. While there are different forms of Progeria, the most sever form of progeria is formally known as Hutchinson-Gilford Progeria Syndrome, which was named after the doctors in England: in 1886 by Dr. Jonathan Hutchinson who described the syndrome, and by Dr. Hastings Gilford who independently discovered it in 1904 (Jameson).

How is it possible for a child to be born looking healthy to then rapidly age and die at an early age? Progeria, a genetic disease, is the answer. This rare disease causes premature aging and is fatal. By looking at the symptoms, the genetic cause, the research for a cure, and what you can do it, is possible to understand progeria.

Progeria, also known as Hutchinson Gilford Progeria Syndrome, and Progeria syndrome, is an extremely rare genetic disease wherein symptoms resembling aspects of aging are manifested at a very early age. The Progeria come from the Greek words “pro” meaning “before” and “gēras” meaning “old age”. The disorder has a very low incident rate, occurring in an estimated 1 per 8 million live births. Those born with Progeria typically live to their mid teens and early twenties. It is a genetic condition that occurs as a new mutation, and is rarely inherited. Although the term Progeria applies strictly to all diseases characterized by premature aging symptoms, and is often used as

It is not only important to take care of our spiritual bodies, we must care for our physical bodies as well. Younger people are experiencing chronic diseases and, as a result, having their lives cut short. A key factor leading to such diseases is being overweight or obese, especially during childhood because such habits can continue into adulthood.

Progeria, also known as Hutchinson-Gilford Progeria Syndrome (HGPS) is an extremely rare genetic disorder where symptoms resembling aspects of aging are displayed at a very early age (Progeria 101). A genetic disease is an illness caused by one or more abnormalities in the genome, especially a condition that is congenital (present from birth). Genetic diseases are rare and may or may not be heritable. There are thousands of extremely rare genetic diseases, one being Progeria. Progeria affects its victims and their families more than physically; it takes a toll on the mental and emotional state of mind.

The aging process in late adulthood is called senescence. People cannot stop the effects of aging but there are alternatives that can help ease the process. These measures are not always followed because people make poor life choices such as smoking. Aging adults will even spend millions of dollars trying to slow the process of aging. No matter how much money they spend aging will occur.

The type of Progeria Sam had is called Hutchinson-Gilford Progeria Syndrome, “child Progeria” rather than Werner’s syndrome, also know as “adult Progeria”, that does not occur until late teens, resulting in longer lives into the 40’s-50’s (“Progeria 101/FAQ"). Progeria has a vast amount of symptoms that the majority of those suffering deal with as well as symptoms that are seen less often. Throughout early infancy, children with Progeria resemble normal infants’ physical appearance. Around age 1 or 2 they begin to display extreme growth delay causing them to be short, and have low weight. Their faces appear to be small compared to their head size; furthermore, their faces seem shrunken, wrinkled, and slender. Skulls will have visible veins along the forehead, nose-bridge, as well as the other areas across the head. Other symptoms include having a small jaw, delayed or failed tooth development, deformity of teeth with crowding, beaked nose, prominent eyes, brittle nails, dislocated hips, skeletal defects, and loss of hair, eyebrows, and eyelashes (Chandravanshi et al.). More damaging symptoms are atherosclerosis (hardening of the arteries), cardiovascular issues (strokes heart attacks), arthritis, and osteoporosis (“Progeria 101/FAQ"). The children who have Progeria are very similar in appearance with little effects from various ethnicities (“Progeria 101/FAQ"). Normally the complications of atherosclerosis lead to the deaths of the children around

Progeria is a disease of children that produces rapid aging. The exact cause of progeria is

Hutchinson-Gilford progeria syndrome is a very rare genetic disorder that causes the affected individuals to appear older than what they are. Individuals are able to be affected by this disorder as earlier as a their first few months of life. There have been reported cases of infection seen in the fetus. Characteristics of progeria include limited growth such as short stature and low body weight, full body hair loss, and facial features that resemble an aged person. This genetic disorder can lead to other health complications such as degeneration of bone mass and tissue, scleroderma, kidney failure, loss of eye sight, atherosclerosis, and severe cardiovascular problems. There is a genetic test to diagnosis the disorder at a younger age called HGPS. Currently, there is no cure or treatment for the disease. However, patients can undergo certain surgeries such as

Progeria is a fatal genetic condition characterized by an appearance of accelerated aging children. There are different types of Progeria but the classic type is Hutchinson-Gilford Progeria Syndrome. Progeria means “prematurely old.” The scientific name for the genetic mutation is Hutchinson-Gilford syndrome, but is known as Progeria or HGPS. HGPS is caused by a mutation of the LMNA gene. The LMNA gene produces the Lamin A protein, which holds the nucleus together, Researchers say that Lamin A protein makes the nucleus unstable which leads to aging in Progeria. The symptoms of Progeria in the skin are wrinkles or dryness. Some common symptoms of Progeria are hair loss, delayed tooth development, enlarged head, high-pitched voice, loss of muscle,

Aging is an unavoidable stage of the body lifespan, which results in lower physiologic capacities, lower homeostasis, and high vulnerability to acquire diseases. Aging changes generally occur later in life, but one in every four or eight million newborns are born with Hutchinson Gilford Progeria Syndrome (HGPS), and manifestation of advance age related diseases like thin skin, osteoporosis, cardiovascular diseases, etc. Progerias is identified by physical and clinical features that portray premature ageing. This syndrome is a rare and fatal genetic disorder identified by accelerated premature ageing and extremely fast developed cardiovascular diseases.

Hutchinson-Gilford progeria syndrome is a genetic disorder that causes the appearance of young children to intensely and rapidly age and have illnesses that are typically associated with the elderly. Progeria is caused by a mutated gene called the LMNA and this gene produces a protein called lamin-a. Lamin-a is an important protein because it is what’s responsible for creating the shapes of the nucleus in cells. It’s also responsible for supporting the nuclear envelope, which is the membrane that surrounds the nucleus. Progeria is caused because of the creation of an abnormal version of the lamin-a protein.

Progeria is a syndrome in individuals which causes physical signs and symptoms of premature old age. Progeria is a very rare and fatal disease. The syndrome’s name is Greek and means “prematurely old”. There are a few different types of progeria but the most common or “classic” type is called Hutchinson-Gilford Progeria syndrome. This was named after the doctors in England who first discovered and described progeria, Dr. Jonathon Hutchinson in 1866 and Dr. Hastings Gilford in 1897.

Progeria is a syndrome that is extremely rare which causes premature aging in children. I found this disease very interesting because infants appear perfectly normal at birth but the aging process begins to happen very rapidly as early as 12 months. The young children will start displaying elderly characteristics as the disease progresses. These children will often die from old age diseases such as heart attacks, and strokes or related complications. The mayo clinic website indicates that progeria children live an average of 13 years, some can live up to 20 or more. The oldest living progeria patient recorded was Meg Casey who according to the Orlando Sentinel newspaper died in Connecticut at 29 years old. Progeria, also known as

Through reading this article in Zone 1 of the Centre you will gain a deeper understanding into how looking after your health can protect you from developing a whole range of health conditions as you get older (some of them life-threatening diseases and conditions). You will learn what 'taking care of yourself ' actually means from a physiological and psychological standpoint. And you will also discover how you can combine the right diet with a regular exercise activity to suit you, so that every day you are strengthening your shield against the onset of poor health as you grow older.