Progeria is an extremely rare disease affecting only about 1 in 4 million babies born worldwide. According to the Progeria Research Foundation’s website, there are currently 105 known cases in 38 countries worldwide. Since this disease is a sporadic autosomal dominant condition only one copy of the mutated gene is sufficient to cause the disorder. Progeria occurs mostly in people with no history of the disorder. Gene mutations know neither race nor sex, therefore this disease non-bias to race or sex and will occur with equal likelihood across all nationalities. The likely reason that this disease is so rare is because the gene cannot be passed on due to young age that this disease fatally attacks.
Pre-symptom tests are available, however due to the rarity of the disease and sporadic nature of its occurrence, pre-symptom ...
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...Progeria, heart disease and aging. PRF has its own Cell and Tissue Bank that provides the biological materials researchers need to conduct their experiments. Additionally, PRF has established a Medical and Research Database to supply physicians and families with medical recommendations for cardiac care, nutrition and other medical issues to help children and adults with Progeria have a better quality of life. In April 2010, PRF published The Progeria Handbook for families and doctors. From basic health facts to daily care recommendations to extensive treatment guidelines, the handbook helps answer many questions for people suffering from Progeria throughout the world. Supporting research foundations like PRF will lead to a cure for Progeria and may provide keys for treating millions of adults with heart disease and stroke associated with the natural aging process.
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- Hutchinson-Gilford Progeria Syndrome, also known as “Progeria,” is a genetic disease that causes accelerating symptoms of aging in children (Progeria: Hutchinson-Gilford Progeria, 2007). Though extremely rare, this devastating disease is universally fatal. The purpose of this paper is to examine the causes, effects, and current treatments of this deadly disease. Progeria occurs due to a mutation in the LMNA gene. In normal cells, this gene encodes the structural protein lamin A. Lamin A, along with lamin B and lamin C, is a supporting component of the nuclear envelope (The Science Behind, 2014).... [tags: Progeria, genetic disease, accelerating]
1074 words (3.1 pages)
- 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. Yet, I have never even heard of it till now. Hutchinson Gilford Progeria Syndrome is a rare genetic disorder. It was discovered in 1886 by Hastings Gilford and Jonathan Hutchinson. It did not gain people’s attention though until 1981.... [tags: disease, genetic, disorder]
890 words (2.5 pages)
- Progeria is a rare, untreatable disease that causes children to age prematurely. It is a sickness that affects only a slight amount of people, but needs to be recognized as a severe disorder that affects the body. In the year 1886, Jonathan Hutchinson was researching the symptoms of a six year old boy who appeared to look older than he actually was. Hutchinson kept documentations of this boy and stated that he lost his hair and got wrinkled, veiny skin. Eleven years later, Hutchinson introduced the disease as “progeria” which derives from the Greek word “progeros,” meaning prematurely old.... [tags: Disease, Ageing Prematurely]
982 words (2.8 pages)
- Never judge a book by its cover. Don’t assume a person with wrinkly skin, age spots, or balding scalps are old. They could be struggling with an extremely rare disease known as Hutchinson-Gilford Progeria. One summer I was extremely bored. I went on youtube clicking on random videos until I ended up on a documentary on Progeria. As I watched, I became so intrigued. Hutchinson-Gilford Progeria Syndrome ("Progeria", or "HGPS") is a rare, terminal genetic disease characterized by accelerated aging in children.... [tags: genetic disease, medical condition]
937 words (2.7 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. In 1904 Gilford described a second case of Progeria, thus creating the term to reflect the syndrome’s senile features. There are only about a hundred reported cases since the disorder has been discovered over a century ago. Currently, there are about thirty to forty known cases worldwide of Progeria.... [tags: genetic childhood disorder]
1730 words (4.9 pages)
- Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare fatal genetic disease characterized by rapid aging in early life. It is caused by a recurrent de novo point mutation in Lamin A, where there is a change from glycine GGC to glycine GGT, in codon 608 of lamin A (LMNA) gene, within exon 11 (Eriksson et al., 2003). This mutation causes a truncated splicing mutant of lamin A, called progerin. The accumulation of progerin leads to various ageing-associated nuclear defects including disorganization of the nuclear lamina, disruption of nucleocytoplasmic transport, loss of heterochromatin, DNA damage with a loss of repair efficiency, and premature senescence (Liu, 2005).... [tags: ]
2979 words (8.5 pages)
- ... The emotional backlash of Progeria can be much more profound than the physical. Even though they are different, many children with Progeria are just as happy as normal children their age. They are capable of living every day to its fullest and looking at the positive side of every situation. Sam Berns was a young boy with Progeria. At age thirteen, he gave an interview and stated, “No matter what problems we are facing, there's always room for happiness in our lives” (Foxborough). Like any other child, these children just want to live a normal childhood filled with joy and happiness.... [tags: rare genetic disorders]
1330 words (3.8 pages)
- Hutchinson-Gilford Progeria Syndrome Progeria is a genetic disease in which young children have the appearance of premature aging. The disease named by Dr. Jonathan Hutchinson and Dr. Hastings Gilford who were the first doctor’s to discover the disease in 1886 and 1904. Today, more than six million children are born with progeria all over the world. Progeria is a very complex disease, and this paper will be covering what the signs and symptoms are, what causes progeria, treatments, daily life of a person who suffers from progeria, the prognosis of a person with progeria.... [tags: symptoms, genetics, fatal]
778 words (2.2 pages)
- Progeria is a rare disease that affects two hundred to two hundred and fifty children worldwide. Children with progeria have facial features of an aging person and suffer from many bone abnormalities, inability to gain weight, and cardio vascular disease which is responsible for their deaths. Progeria is caused by a mutation in the LMNA gene which is located in the nuclear membrane. The LMNA gene synthesizes lamin A and lamin C proteins. The intermediate filament proteins are responsible for nuclear stability and strength.... [tags: rare child's genetic disease, premature aging]
1459 words (4.2 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 is a rare condition but has come into public awareness because of its startling symptoms and the appearance of several affected children in movies on national television.The children are small and thin with disproportionately large appearing heads, baldness, wizened narrow faces, and old-appearing skin.... [tags: Papers]
935 words (2.7 pages)
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