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         Progeria:     more books (16)
  1. Kimberly Akimbo by David Lindsay-Abaire, 2003-12
  2. Forever and Ever by Dan A. Baker, 2009-06-01

21. MedlinePlus Medical Encyclopedia: Progeria
progeria is a disease that produces rapid aging, beginning in childhood. progeria is a rare condition that is remarkable because its symptoms strongly
http://www.nlm.nih.gov/medlineplus/ency/article/001657.htm
@import url(/medlineplus/images/advanced.css); Skip navigation
Medical Encyclopedia
Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z
Progeria
Contents of this page:
Illustrations
Coronary artery blockage Alternative names Return to top Hutchinson-Gilford syndrome Definition Return to top Progeria is a disease that produces rapid aging, beginning in childhood. Causes, incidence, and risk factors Return to top Progeria is a rare condition that is remarkable because its symptoms strongly resemble normal human aging, but occur in young children. In addition, the appearance of several affected children in movies and on television have brought progeria to public attention. Ninety percent of children with progeria have a mutation on the gene that encodes the protein lamin A. Progeria usually occurs sporadically, and is not seen in siblings of affected children, although in very rare circumstances more than one child in a family can have progeria. Progeria results in rapid aging of a child, beginning with

22. Redirect
progeria medical database resource for textual information, pictures, and reference information.
http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?176670

23. Progeria (Hutchinson-Gilford) Syndrome
a CHORUS notecard document about progeria (HutchinsonGilford) syndrome
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

24. MedlinePlus Enciclopedia Médica: Progeria
Translate this page La progeria es un padecimiento raro que se destaca por los síntomas, Noventa por ciento de los niños con progeria tienen una mutación en el gen que
http://www.nlm.nih.gov/medlineplus/spanish/ency/article/001657.htm
@import url(/medlineplus/images/advanced.css); Omita y vaya al Contenido
Otros temas: A-Ag Ah-Ap Aq-Az B-Bk ... Z
Progeria
Contenido:
Obstrucci³n de las arterias coronarias Nombres alternativos Volver al comienzo S­ndrome de Hutchinson-Gilford Definici³n Volver al comienzo Es una enfermedad que produce un envejecimiento r¡pido, que comienza en la ni±ez. Causas, incidencia y factores de riesgo Volver al comienzo La progeria es un padecimiento raro que se destaca por los s­ntomas, que se asemejan bastante al envejecimiento humano normal, aunque se presenta en ni±os peque±os. Adem¡s, la aparici³n de varios ni±os afectados en pel­culas y en televisi³n ha llamado la atenci³n del pºblico. Noventa por ciento de los ni±os con progeria tienen una mutaci³n en el gen que codifica la prote­na Lamin A. La progeria generalmente ocurre en forma espor¡dica y no se observa en hermanos de ni±os afectados, aunque, en circunstancias muy poco comunes, m¡s de un ni±o en una familia puede tener esta enfermedad. La progeria produce un r¡pido envejecimiento de los ni±os, comenzando con una

25. Edpage.html
Welcome to My Web Page on progeria! lots of love to give, who has progeria. What is progeria? progeria, also known as HutchinsonGilford
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

26. Progeria Syndromes
Article describes the progeria syndromes, their symptoms, and possible causes.
http://rarediseases.about.com/cs/progeriasyndromes/a/060803.htm
var zLb=12; var zIoa1 = new Array('Suggested Reading','More about Werner syndrome','http://rarediseases.about.com/od/rarediseasesw/a/100304.htm'); var zIoa2 = new Array('Elsewhere on the Web','Progeria Research Foundation','http://www.progeriaresearch.org'); zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a70' About Rare / Orphan Diseases Rare Diseases O - R Rare Diseases: P - Q Progeria Syndromes Rare Diseases Essentials Rare Diseases: Basic Information Rare Diseases Support Groups ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb);
FREE Newsletter
Sign Up Now for the Rare / Orphan Diseases newsletter!
See Online Courses
Search Rare / Orphan Diseases Stay up to date! Compare Prices Email to a friend ... Print this page
Suggested Reading More about Werner syndrome Elsewhere on the Web Progeria Research Foundation Most Popular Muscular Dystrophy ALD and Lorenzo's Oil Progeria Syndromes Leprosy (Hansen's Disease) ... The Elephant Man What's Hot Charcot-Marie-Tooth Disease Peyronie's Disease Twin-to-Twin Transfusion Synd Autoimmune Kidney Disease ... Cri-du-Chat Syndrome adunitCM(150,100,'x55')

27. Sunshine Foundation Home
Refer A Child Donate Dream Village progeria Dreamlifts News Adopt A Dream FAQ Events Contact IMPORTANT!
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

28. Progeria Syndromes
Links to information and support for progeria syndromes, including HutchinsonGilford and Werner.
http://rarediseases.about.com/cs/progeriasyndromes/
zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a70' About Rare / Orphan Diseases Rare Diseases Essentials ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb);
FREE Newsletter
Sign Up Now for the Rare / Orphan Diseases newsletter!
See Online Courses
Search Rare / Orphan Diseases Progeria syndromes
Guide picks Syndromes involving premature aging. Hutchinson-Gilford syndrome begins in infancy, and Werner syndrome begins in adulthood.
Progeria Syndromes

This disorder, in which tumors grow throughout the body, ranges from mild, almost undetectable, effects to severe impairment. From the About.com Guide to Rare/Orphan Diseases. Hutchinson-Gilford Progeria Syndrome Resource Center
Information, photos, and discussion forum. Lori and Ashley's Website
Personal site devoted to family affected by Hutchinson-Gilford progeria. Progeria Research Foundation, Inc.
Site offers information, international registry, news, and events. Sunshine Foundation
Non-profit which sponsors yearly worldwide reunion of children with progeria.

29. Hutchinson-Gilford Progeria Syndrome Network
Mon, 31 Jan 2005 New York Times on progeria Wed, 07 Jul 2004 New progeria Research
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

30. Genome.gov | Learning About Progeria
Information about the genetic disease progeria. progeria is an extremely rare genetic disease of childhood characterized by dramatic, premature aging.
http://www.genome.gov/11007255
triggerParms["cpp_5"] = "Referer:"+ cppUrlPatch (""); // Optional Home About NHGRI Newsroom Staff ... Specific Genetic Disorders Learning About Progeria
Learning About Progeria
Read About NHGRI's Latest Research: Anti-Cancer Drugs May Hold Promise for Premature Aging Disorder What do we know about heredity and progeria? Is there a test for progeria? NHGRI Clinical Research on Progeria ... Additional Resources for Progeria Information
What do we know about heredity and progeria?
Progeria is an extremely rare genetic disease of childhood characterized by dramatic, premature aging. The condition, which derives its name from "geras," the Greek word for old age, is estimated to affect one in 8 million newborns worldwide. The most severe form of the disease is Hutchinson-Gilford progeria syndrome, recognizing the efforts of Dr. Jonathan Hutchinson, who first described the disease in 1886, and Dr. Hastings Gilford who did the same in 1904. As newborns, children with progeria usually appear normal. However, within a year, their growth rate slows and they soon are much shorter and weigh much less than others their age. While possessing normal intelligence, affected children develop a distinctive appearance characterized by baldness, aged-looking skin, a pinched nose, and a small face and jaw relative to head size. They also often suffer from symptoms typically seen in much older people: stiffness of joints, hip dislocations and severe, progressive cardiovascular disease. However, various other features associated with the normal aging process, such as cataracts and osteoarthritis, are not seen in children with progeria.

31. MedlinePlus Medical Encyclopedia Progeria
progeria is a disease that produces rapid aging, beginning in childhood. Causes, incidence, and risk factors Return to top
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

32. Progeria / The Family Village
each year Sunshine sponsors a worldwide reunion of children suffering from progeria. The progeria Reunion gives those children suffering from this rare
http://www.familyvillage.wisc.edu/lib_prog.htm
Progeria
Also known as Hutchinson-Gilford Progeria Syndrome
Who to Contact
Where to Go to Chat with Others

Learn More About It

Web Sites
...
Search Google for "Progeria"
Who to Contact
Sunshine Foundation Dream Village (Main Office)
5400 C.R. 547 North
P.O. Box 255
Loughman, FL 33858
E-mail: florida@sunshinefoundation.org
Website: http://www.sunshinefoundation.org/progeria.html Since 1976 The Sunshine Foundation® has fulfilled over 23,500 dreams and wishes for chronically ill, terminally ill, and abused children. Whether it's a visit with a celebrity hero, a family outing, a trip to Disney World® or a special gift Sunshine has never said "no" to a deserving child. The majority of wishes Sunshine fulfils are to visit Central Florida attractions. Therefore in February of 1990 Sunshine opened the doors of its' Dream Village and since then approximately 1000 special children and their families have enjoyed the facilities at this special place for special children. In a fairytale like setting with a gingerbread facade, the Sunshine Foundation Dream Village is a place where children and their families stay while they briefly forget the pain and suffering that is part of their everyday lives. In addition, each year Sunshine sponsors a worldwide reunion of children suffering from Progeria. The Progeria Reunion gives those children suffering from this rare disease the opportunity to meet and get to know others with this rare genetic disease.
International Progeria Registry W.T. Brown, MD, Ph.D.

33. Sunshine Foundation | Home
progeria Reunion! Each year Sunshine Foundation holds a reunion, which brings together children from all over the world with the rare aging disease known as
http://www.sunshinefoundation.com/
Refer A Child Donate Dream Village Progeria ... Check out the great photos from the 1st Annual Sunshine for Kids Golf Tournament IMPORTANT!
As of January 1st, 2005, please note changes to our guidelines - Click here and look under Criteria
Get your

Sunshine Wristband
...
a piece!

DENZEL
, age 12, lives in Manhattan, NY. He is blind and suffers from cerebral palsy. Denzel loves music and enjoys entertaining his family by playing his keyboard.
FRANCISZEK , age 12, Lawrence, MI wants to be an engineer when he grows up. Franciszek has cerebral palsy with dysplasia. He enjoys swimming and playing with his two dogs and two cats.
CARLOS , age 18, from Los Angeles, CA has Leukemia A.L.L.. Carlos really enjoys using his computer for research. This will come in very handy, as he plans to become a lawyer one day.

DONATE

TOWARDS A

DREAM
document.write(""); A Great Loss for Our Progeria Family Stuart and Ronny leave behind countless, beautiful moments that will live in our hearts forever.

34. Progeria FAQ
progeria is commonly referred to as an early aging disease. progeria is an autosomal recessive disease, meaning that an individual carrying a mutation
http://www.seps.org/cvoracle/faq/progeria.html
Progeria FAQ
What is it?
Progeria is commonly referred to as an "early aging disease." Although whether early aging actually occurs or whether this is a disease with many symptoms that look like aging is debated. It is also known as Hutchinson-Gilford progeria syndrome (HGPS), named after Jonathan Hutchinson, who first described the disease in 1886 and Hastings Gilford (1904), who was the first to refer to the disease as progeria ( National Library of Medicine, Progeria ). It is fortunately an extremely rare disease. Only somewhat more then 100 cases have been reported since it was discovered, and is estimated to affect only 1 to 2 children in 8 million. It is, however, a particularly tragic disease in that it typically strikes children before the age of 10 years, who then usually die before their teens. Patients have some characteristics of aging such as baldness, a pinched nose, delayed tooth formation, stiffness of joints, hip dislocations, cardiovascular problems, arteriosclerosis, wrinkled/aged-looking skin, and a premature cessation of growth (dwarfism). They do not, however, typically show other characteristics of aging such as Alzheimer's disease, and arthritis of the hips in these patients is a result of having been born with dislocated hips, not as an aging process. Werner syndrome is a similar appearing disease, but it strikes people in their late teens. These patients may live until their 40s. Symptoms include scaly changes, especially in the extremities, cataracts, subcutaneous calcification, premature arteriosclerosis, diabetes mellitus, and wizened and prematurely aged facial features (

35. Progeria (Hutchinson-Gilford) Syndrome
a CHORUS notecard document about progeria (HutchinsonGilford) syndrome.
http://chorus.rad.mcw.edu/doc/00334.html
CHORUS Collaborative Hypertext of Radiology Multisystem entities About CHORUS
Search

Feedback
progeria (Hutchinson-Gilford) syndrome
premature aging in children
  • normal at birth
  • "wizened old man": alopecia, atrophy of muscles and skin
  • atherosclerosis ==> coronary artery disease
  • dwarfism
  • abnormal facies: receding chin, beaked nose, exophthalmos
Findings: Charles E. Kahn, Jr., MD - 2 February 1995
Last updated 26 May 2004
Related CHORUS documents:
acro-osteolysis Wormian bones achondroplasia pulmonary embolism ... syndromes of paranasal sinuses
Search for related articles:
AJR American Journal of Roentgenology PubMed : index to biomedical literature ...

Medical College of Wisconsin

36. Progeria (Hutchinson-Gilford) Syndrome
progeria (HutchinsonGilford) syndrome. premature aging in children. normal at birth; wizened old man alopecia, atrophy of muscles and skin
http://chorus.rad.mcw.edu/to-go/00334.html
progeria (Hutchinson-Gilford) syndrome
premature aging in children
  • normal at birth
  • "wizened old man": alopecia, atrophy of muscles and skin
  • atherosclerosis ==> coronary artery disease
  • dwarfism
  • abnormal facies: receding chin, beaked nose, exophthalmos
Findings: Home Multisystem entities

37. Progeria Syndrome
progeria syndrome information, national and international support groups, clinics with genetic counselors, geneticists.
http://www.kumc.edu/gec/support/progeria.html
Progeria syndromes
(Hutchinson-Gilford Syndrome, Werner Syndrome, Cockayne Syndrome, Rothmund-Thomson Syndrome)
Progeria Research Foundation
P.O. Box 3453 Peabody, MA 01961-3453 Phone: 978.535.2594 Fax: 978.535.5849 E-mail: progeria@netzero.net Web site: www.progeriaresearch.org/ Friends of Progeria Foundation , Huron, SD
The Sunshine Foundation (for children with terminal, chronic illnesses such as progeria, dedicated to making the dreams of these children possible)
1041 Mill Creek Drive Feasterville, PA 19053 Phone: 1.800.767.1976 or 215.396.4770 Fax: 215.396.4774 E-mail: philly@sunshinefoundation.org Web site: www.sunshinefoundation.org/
Sunshine Foundation, Dream Village
PO Box 255, 5400 C.R. 547 North Loughman, FL 33858 Phone: 800.457.1976 or 863.424.4188 Fax: 863.424.4360 E-mail: florida@sunshinefoundation.org Web site: www.sunshinefoundation.org/dreamvillage.html Sunshine Foundation, Volunteer Chapters California, Colorado, Delaware, District of Columbia, Georgia, New Jersey, Pennsylvania, West Virginia
Black Hills (PO Box 5009, Rapid City, SD 57709-5009, Phone: 605.393.0426, Fax: 605.393.1369, Fax On Demand: 605.393.0426, option 10)

38. HONselect - Progeria
English, progeria, Hutchinson-Gilford Syndrome - Hutchinson Gilford Syndrome Português, progeria, - Síndrome de Hutchinson-Gilford
http://www.hon.ch/HONselect/RareDiseases/C18.452.648.769.html
List of rare diseases: English Deutsch
Language:
MeSH term:
Accepted terms:
English: Progeria - Hutchinson-Gilford Syndrome
- Hutchinson Gilford Syndrome
- Syndrome, Hutchinson-Gilford
Français: Progeria - Gilford, syndrome
- HGPS
- Progérie de Hutchinson-Gilford
Deutsch: Progerie - Hutchinson-Gilford-Syndrom - Zwergwuchs, greisenhafter - Gilford-Syndrom - Paedogerie Español: Progeria - Síndrome de Hutchinson-Gilford Português: Progeria - Síndrome de Hutchinson-Gilford HONselect ressources Definition: Yes Articles: Yes Images: No News: No Conferences: No Clinical trials: Yes Web sites: English Yes Français Yes Deutsch Yes Español Yes Português No Home About us Site map Search ... Contact http://www.hon.ch/HONselect/RareDiseases/C18.452.648.769.html Last modified: Wed May 18 2005

39. Progeria - Gilford, Syndrome HONsélect
progeria articles, sites web, images, Nouvelles médicales pour progeria (en anglais seulement). Pas de résultats pour ce terme.
http://www.hon.ch/HONselect/RareDiseases/FR/C18.452.648.769.html
InitBulle("navy","#F8F8F8","#000066",1); sites HONcode sites Web HONsélect News ... Images Chercher HONsélect Anglais Français Allemand Espagnol Portugais
le mot la partie du mot dans les termes MeSH Information pour "Progeria": Hiérarchie médicale et definition Articles médicaux Ressources du Web Images médicales Nouvelles médicales Conférences médicales Hiérarchie Anglais Français Allemand Espagnol Portugais
Progeria Définition: An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature greying; hair loss; hearing loss ( DEAFNESS ); cataracts ( CATARACT ARTHRITIS OSTEOPOROSIS DIABETES MELLITUS ; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID ; and accelerated ATHEROSCLEROSIS . Many affected individuals develop malignant tumors, especially SARCOMA
Synonyme(s): Gilford, syndrome / HGPS / Progérie de Hutchinson-Gilford /
Voir également: Cockayne, syndrome Syndrome de Werner
Voir connexe: Sarcome Arthrite Ostéoporose Artériosclérose ... Lamine A
(NLM)®
de l'INSERM (version française)
Parcourir
Chercher HONsélect
Ressources du Web pour "Progeria" Anglais = Site with HON description - = Site with a robot description info: entrez dans le site: (cliquez ci-dessous) domaine du site: HONcode - Progeria - ORPHANET - Maladies rares - Médicaments orphelins www.orpha.net

40. Fight Aging!: On Progeria
After discovering the genetic roots of progeria, modern bioinformatics made it the Further research into understanding and curing progeria and related
http://www.fightaging.org/archives/000251.php
"We are on the verge of a revolution in medicine: understanding, treating, and ultimately preventing the causes of degenerative aging. But medical revolutions only happen if we all stand up in support of funding and research. We did it for cancer. We're doing it for Alzheimer's. We can do it for aging - and create an era of longer, healthier lives!" Search Required Reading Calorie Restriction
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