Progeria disease essay

Progeria - hutchinson-gilford syndrome essay 1734 words | 7 pages progeria, otherwise known as hutchinson-gilford syndrome is an extremely rare, genetic childhood disorder with a reported incidence of about one in a million hutchinson reported the syndrome in 1886 when he found the first patient with progeria. Progeria disease progeria also referred to as hutchinson-gilford syndrome (hgs), is a tremendously rare, progressive heritable condition, which makes children to quickly age, starting in their initial two years of their life normally, these children are normal at birth, but signs and symptoms start to appear in their first year of life. Werner syndrome is also known as progeria adultorum, progeria of the adult and pangeria it is the most common of the premature aging disorders it is the most common of the premature aging disorders. Progeria is a rare, fatal, sporadic, autosomal dominant syndrome that involves premature aging, generally leading to death at approximately 13 years of age due to myocardial infarction or stroke.

progeria disease essay Progeria is a genetic disorder rarely encountered and is characterized by features of premature aging 2 it is also known as “hutchinson-gilford progeria syndrome” in this syndrome, the rate of ageing is accelerated up to seven times that of normal.

Progeria (from the greek “pro” means “over”, “gerontos” – “an old man”) is an extremely rare genetic disease, accelerating the process of aging approximately at 7-12 times in other words, in a year of life the child grows old as in 10 years. Progeria essay 950 words | 4 pages progeria progeria is a disease of children that produces rapid aging the exact cause of progeria is unknown, although a hereditary component may be involved progeria results in rapid aging of children, beginning with growth failure during the first year of life. Progeria, the premature fatal aging disorder in children, may be able to be reversed through farnesyltransferase inhibitors (fti) treatments formally known as hutchinson - gilford syndrome, progeria is a genetic disorder that affects 1 in every 8 million babies born the disorder is known for its unusual appearance of premature aging in children.

The disease is called progeria (also known as hutchinson-gilford progeria syndrome) progeria is a very rare terminal condition progeria , affects both males and females of all ethnic backgrounds.

Progeria is named after jonathan hutchinson, who first described the disease in 1886 and hastings gilford who was the first to refer to the disease as progeria progeria is a rare, fatal genetic condition characterized by an appearance of accelerated aging in children it is caused by a mutation in the gene called lmna the lmna gene produces the lamin a protein, which is the structural scaffolding that holds the nucleus of a cell together. Progeria is derived from the greek work meaning prematurely old jonathan hutchinson and hastings gilford discovered the syndrome in 1886 the name hutchinson gilford progeria syndrome existed because of this doctors have discovered a single gene mutation responsible for hutchinson-gilford progeria syndrome. The name hutchinson gilford progeria syndrome existed because of this doctors have discovered a single gene mutation responsible for hutchinson-gilford progeria syndrome the gene is called lamin a this is the protein necessary for holding the center of a cell together. Wtargets derived from the disease models such as the hutchinson gilford progeria syndrome were reviewedtargets derived from the disease models such as the hutchinson gilford progeria syndrome were reviewed pubmedthis essay argues that 20/20 tv nbsp a news magazine series featuring stories involving science, medicine, the arts, news.

This essay evaluates the disease epidemiology of the progeria disease furthermore, this essay seeks to evaluate what factors lead to the development of the condition, and what treatment options are available. Progeria hutchinson gilford syndrome (hgp syndrome) is a genetic condition that is fatal and is characterized by the child developing features of premature ageing it tends to affect the musculoskeletal system, skin and the blood vessels.

Progeria disease essay

progeria disease essay Progeria is a genetic disorder rarely encountered and is characterized by features of premature aging 2 it is also known as “hutchinson-gilford progeria syndrome” in this syndrome, the rate of ageing is accelerated up to seven times that of normal.

Progeria essay examples & outline are you in high school, college, this essay evaluates the disease epidemiology of the progeria disease furthermore, this essay seeks to evaluate what factors lead to the development of the condition, and what treatment options are available the essay also focuses on the arising issues with respect to the. Progeria, the premature fatal aging disorder in children, may be able to be reversed through farnesyltransferase inhibitors (fti) treatments formally known as hutchinson - gilford syndrome, progeria is a genetic disorder that affects 1 in every 8 million babies born. - progeria the genetic disorder i chose is called hutchinson gilford progeria syndrome it is more commonly known as just progeria i chose to write my paper on progeria because it is a disease that many people know about, because its been on the news, and made into books and movies.

As with any person suffering from heart disease, the common events for progeria children are strokes, high blood pressure, angina, enlarged heart, and heart failure, all conditions associated with aging “these children get heart disease at an incredibly accelerated pace, usually y the time they are 12, 13 or 14.

progeria disease essay Progeria is a genetic disorder rarely encountered and is characterized by features of premature aging 2 it is also known as “hutchinson-gilford progeria syndrome” in this syndrome, the rate of ageing is accelerated up to seven times that of normal. progeria disease essay Progeria is a genetic disorder rarely encountered and is characterized by features of premature aging 2 it is also known as “hutchinson-gilford progeria syndrome” in this syndrome, the rate of ageing is accelerated up to seven times that of normal.
Progeria disease essay
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