1. The Progeria Project Foundation - It S About Time - This Web A group concerned about the wellbeing and quality of life for progeria children and their families. http://www.progeriaproject.com/

2. Progeria - Welkom Op De Website Van Michiel - Last Updated: 30.08.2005 Persoonlijke site van ouders met een kind dat lijd aan progeria. Informatie over deze aandoening, foto album en relevante links. http://www.progeria.centerall.com/

Progeria - Welkom op de website van Michiel - Last updated: 30.08.2005 Home Contact Identiteit Michiel Informatie Progeria ... Gastenboek English Version Progeria Michiel English Michiel : de grootste liefde van ons leven Door Godelieve Wielemans en Wim Vandeweert, de zeer trotse ouders van Michiel. (Wonende in België) Toen Wim en ik trouwden, wilden wij net zoals zovelen trouwen, huisje bouwen en een gezinnetje stichten.  Op een gegeven moment vonden wij de tijd rijp om aan het gezinnetje te beginnen.  Een eerste keer in verwachting: joepie!  Echter helaas; deze liep in een miskraam uit.  Enige maanden later opnieuw: joepie!  Wij kregen een kindje!  Opnieuw de teleurstelling en het verdriet toen het wederom misging.  Heel veel traantjes gelaten.  Ja, derde keer goede keer dachten wij!  Extra voorzichtig.  Goede zwangerschap achter de rug, niet te veel ziek geweest en na een paar maanden héél blij want de vrucht zat er nog.  Het was niet misgegaan deze keer. Iedere dag een beetje blijer en jawel hoor: op 13 juni 1998 ziet Michiel het eerste levenslicht in het ziekenhuis te Hasselt tijdens de voetbalmatch België – Nederland.  Regelmatig moest de verpleegster van de dokter en van Wim gaan horen wie er voor stond en wie ging winnen.  Heel spannend allemaal terwijl het mij op dat moment geen bal scheelde want ik stond op het punt om voor het eerst “mama” te worden.  Na een gewone, rustige bevalling was hij daar.  Toen ik hem voor het eerst in mijn armen had, kreeg ik zo een zalig gevoel over mij.  Ik lag op een wolk te drijven; zo héérlijk voelde ik mij met mijn jongen in mijn armen.

3. NORD - National Organization For Rare Disorders, Inc. Outlines the symptoms and lists related organizations. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Progeria, Hut

4. Niederländische Version Stichting voor kinderen met progeria, met informatie over deze aandoening en contact informatie. http://www.progeriafamilycircle.de/holl/

window.open('http://ptbanner.gmx.de/werbungpt1.php3?domain=progeriafamilycircle.de','pt6ds17brXRHM','width=488,height=50'); STICHTING VOOR KINDEREN MET PROGERIA Wij hopen een steentje bij te dragen aan het levensgeluk en de levenskwaliteit van kinderen met Progeria Op deze site vindt u veel informatie over de ziekte PROGERIA, een aandoening die bij kinderen verschijnselen van vroegtijdige veroudering veroorzaakt. Progeria is ook wel bekend onder de namen HUTCHINSON-GILFORD of PROGERIA INFANTILITIS. Naast klinische beschrijvingen, diagnostiek, symptomen, mogelijke oorzaken en therapieën vindt u ook persoonlijke verhalen in de vorm van biografieën van Progeriakinderen uit de hele wereld. Mocht u na lezing van de documentatie op deze website nog vragen hebben , of heeft u aanvullende informatie voor ons, dan kunt u zich richten tot : progeriafamilycircle@hetnet.nl . U kunt ons via dit adres schrijven in het Nederlands, Engels, Frans en Spaans. De Progeria Family Circle staat als Stichting voor kinderen met Progeria sinds 1997 in Nederland ingeschreven in het stichtingenregister van de Kamer van Koophandel Utrecht onder (doorkies)nr.S266015. Met een spontane financiële bijdrage zijn wij natuurlijk ook erg blij. Uw gift is fiscaal aftrekbaar, en u kunt er zeker van zijn dat ze volledig en direct ten goede komt aan de kinderen met Progeria in Europa.

5. Index Overview of the rare disorder, symptoms, and experiences of children with progeria and their families. http://www.progeriafamilycircle.de/

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6. Progéria Fiche dinformation pratiques sur  la progeria de HutchinsonGilford, signes de la maladie, autres sites internet et types de consultations. http://www.orpha.net/static/FR/progeria.html

Accès à la base de données Orphanet Progéria Accès direct aux détails Résumé La progeria de Hutchinson-Gilford est une affection caractérisée par un vieillissement prématuré de début postnatal. Les signes cliniques et radiologiques principaux comprennent une alopécie, une peau fine, une hypoplasie des ongles, une absence de graisse sous cutanée, et une ostéolyse. L'intelligence est normale. Les patients décèdent précocement dans un contexte d'athérosclérose, de maladie cérébrovasculaire ou de dénutrition. La plupart des observations sont sporadiques, dues à une mutation de novo tronquante dominante et récurrente du gène LMNA qui code pour la lamine A, et qui a été retrouvée chez la majorité des patients atteints de progeria. Il existe de nombreux syndromes progeroïdes représentant des diagnostics différentiels. *Auteurs : Drs L. Faivre et V. Cormier-Daire (mars 2005)*. Signes de la maladie CHEVEUX RARES/HYPOTRICHIE/ATRICHIE CLAVICULE ANOMALIE DENTS ERUPTION TARDIVE DIFFICULTE D'ELEVAGE DOIGTS PHALANGE DISTALE HYPOPLASIE EXOPHTALMIE FACE ETROITE HYDARTHROSE/ARTHROSE LUXATION DE HANCHE MAIGREUR (AUTRE QUE LIPODYSTROPHIE) ONGLES FINS / HYPOPLASIQUES (PIEDS) ONGLES FINS/HYPOPLASIQUES (MAINS) PEAU FINE PEAU GLABRE / ABSENCE DE POILS PETITE TAILLE / NANISME RAIDEUR ARTICULAIRE RETARD PUBERTAIRE/HYPOGONADISME RETROGNATHISME/MICROGNATHISME SENILITE PRECOCE/VIEILLISSEMENT PREMAT.

7. Progeria Informatie over deze aandoening van Antwerpse verpleegkundigen. http://members.lycos.nl/progeria/

Progeria Welkom Wie zijn wij ? Wat is ''progeria'' ? Eigenschappen van ''Progeria''? De oorzaken van '' Progeria '' ? ... Links Beste bezoekers, Graag heten wij jullie welkom op onze site... heb je nog feed-back of vragen dan kan je mij ( de webmaster) altijd contacteren door naar het volgende e-mail adres te zenden. progeria@lycos.nl Even een korte voorstelling... Hier zullen wij ons even voorstellen. Wij zijn 5 1ste jaars studenten verpleegkunde te Antwerpen. Onze namen zijn Veronick ( webmaster ) Priscilla Stef Ellen Marjan Ons doel van deze website is dat de mensen een andere kijk krijgen over de ziekte '' Progeria '' . * Wat is ''Progeria'' ? * De eigenschappen van ''Progeria'' ? * De oorzaken van ''Progeria'' ? * Is '' Progeria '' zeldzaam ? * De prognose van ''Progeria'' ? * Wat waren onze acties? Dit zijn de soort vragen die we hier samen voor jullie gaan trachten te beantwoorden.

8. Index „gnar sig ¥t fastighetsf¶rmedling och fortbildning. http://www.progeria.se/

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9. The Progeria Research Foundation Homepage progeria Research Foundation conducts the support of Medical Research, Promotion of Education and Awarness, and Fundraising. http://www.progeriaresearch.org/

BREAKING NEWS! STUDIES SHOW POTENTIAL DRUG TREATMENT FOR PROGERIA Researchers have published studies that support a potential drug treatment for children with Progeria. The labs of Dr. Francis Collins at the National Institutes of Health, Dr. Loren Fong at UCLA and Dr. Thomas Glover at U Michigan have produced these exciting results. We're proud that PRF has participated in all of these studies. Click here for details. PRF ANNOUNCES INTERNATIONAL WORKSHOP 2005 Setting the stage for the next round of progress in translating bench research on Progeria into treatment. Click here for details 2005 marks a record year for the advancement of Progeria research. We have eight active research grants in progress, and our , and Diagnostics Testing programs are running full speed ahead. Because of our accomplishments and goals, families and their doctors turn to PRF for medical support, and PRF is regarded worldwide as the leader in Progeria research and education.

10. Hutchinson-Gilford Progeria Syndrome Network Provides an overview of the disease as well as links to resources. http://www.laze.net/progeria/index.html

@import "/hgps.css"; Introduction Hutchinson-Gilford Progeria Syndrome is an extremely rare genetic disease that accelerates the aging process to about seven times the normal rate. Because of this accelerated aging, a child of ten years will have similar respiratory, cardiovascular, and arthritic conditions that a 70-year-old would have. Progeria affects between 1 in 4 million (estimated actual) and 1 in 8 million (reported) children, with a total reported incidence of just over 100 in the century since it's been identified. There are currently between 30 and 40 known cases worldwide of Progeria. Children from all races and cultures around the world have been affected. Physical features of Progeria children include dwarfism, wrinkled/aged-looking skin, baldness, and a pinched nose. Mental growth is equivalent to other children of the same age. Most children with Progeria don't live beyond their early teenage years, though one or two have lived to their early 20s. ... more about Progeria and this site Latest News and Updates Tue, 21 Jun 2005

11. The Progeria Research Foundation Homepage progeria Research Foundation conducts the support of Medical Research, Promotion of Education and Awarness, and Fundraising http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

12. Hutchinson-Gilford Progeria Syndrome Network progeria affects between 1 in 4 million (estimated actual) and 1 in 8 million There are currently between 30 and 40 known cases worldwide of progeria. http://www.hgps.net/

@import "/hgps.css"; Introduction Hutchinson-Gilford Progeria Syndrome is an extremely rare genetic disease that accelerates the aging process to about seven times the normal rate. Because of this accelerated aging, a child of ten years will have similar respiratory, cardiovascular, and arthritic conditions that a 70-year-old would have. Progeria affects between 1 in 4 million (estimated actual) and 1 in 8 million (reported) children, with a total reported incidence of just over 100 in the century since it's been identified. There are currently between 30 and 40 known cases worldwide of Progeria. Children from all races and cultures around the world have been affected. Physical features of Progeria children include dwarfism, wrinkled/aged-looking skin, baldness, and a pinched nose. Mental growth is equivalent to other children of the same age. Most children with Progeria don't live beyond their early teenage years, though one or two have lived to their early 20s. ... more about Progeria and this site Latest News and Updates Tue, 21 Jun 2005

13. The Progeria Research Foundation Homepage Medical research, education, support, and fundraising for this premature aging disease. http://progeriaresearch.org

BREAKING NEWS! STUDIES SHOW POTENTIAL DRUG TREATMENT FOR PROGERIA Researchers have published studies that support a potential drug treatment for children with Progeria. The labs of Dr. Francis Collins at the National Institutes of Health, Dr. Loren Fong at UCLA and Dr. Thomas Glover at U Michigan have produced these exciting results. We're proud that PRF has participated in all of these studies. Click here for details. PRF ANNOUNCES INTERNATIONAL WORKSHOP 2005 Setting the stage for the next round of progress in translating bench research on Progeria into treatment. Click here for details 2005 marks a record year for the advancement of Progeria research. We have eight active research grants in progress, and our , and Diagnostics Testing programs are running full speed ahead. Because of our accomplishments and goals, families and their doctors turn to PRF for medical support, and PRF is regarded worldwide as the leader in Progeria research and education.

14. Progeria Syndrome progeria syndrome information, national and international support groups, clinics with genetic counselors, geneticists http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

15. Hutchinson-Gilford Progeria Syndrome Network :: Index General progeria Discussion. No new posts, General Discussion General discussion about progeria, television programs dealing with progeria, etc. http://www.hgps.net/forum/

Hutchinson-Gilford Progeria Syndrome Network HGPS.net discussion forum FAQ Search Memberlist Usergroups Register Profile Log in to check your private messages Log in The time now is Fri Sep 09, 2005 10:30 am Hutchinson-Gilford Progeria Syndrome Network Forum Index View unanswered posts Forum Topics Posts Last Post General Progeria Discussion General Discussion General discussion about Progeria, television programs dealing with Progeria, etc. Sat Aug 13, 2005 12:32 am Student Discussion Chat with other students about Progeria. Any posts that essentially say "Send me all the information you have!" will be deleted. Thu Aug 04, 2005 2:22 pm Mark all forums read All times are GMT - 5 Hours Who is Online Our users have posted a total of articles We have registered users The newest registered user is Handjobs In total there is user online :: Registered, Hidden and 1 Guest [ Administrator Moderator Most users ever online was on Mon Jan 24, 2005 9:14 pm Registered Users: None This data is based on users active over the past five minutes Log in Username: Password: Log me on automatically each visit New posts No new posts Forum is locked Powered by phpBB

16. Genetic Conditions / Rare Conditions Information Site Porphyria. PraderWilli syndrome. progeria (Werner, Hutchinson-Gilford, Cockayne, Rothmond-Thomson syndromes) Proteus syndrome. Prune belly http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

17. Progeria FAQ HutchinsonGilford progeria Syndrome Research Center, has some good links and family support information. Last updated September 2004 http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

18. The Progeria Project Foundation - Progeria? - What Is Progeria? HutchinsonGilford progeria Syndrome is a very rare progressive disorder of The genetic basis of progeria is uncertain; although a few instances of http://www.progeriaproject.com/Progeria/whatis.htm

Your browser does not support script Progeria? - What is Progeria? Progeria Click here for more information on Progeria. Hutchinson-Gilford Progeria Syndrome Symptoms of the following disorder may be similar to those of Wiedemann-Rautenstrauch Syndrome. Comparisons may be useful for a differential diagnosis: BCHealthGuide http://www.bchealthguide.org Hutchinson-Gilford Disease Also known as: Gilford’s syndrome Hutchinson-Gilford progeria Hutchinson-Gilford syndrome Souques-Charcot syndrome a variant of this syndrome) Synonyms: Premature aging syndrome, premature senility syndrome, progeria, progeria infantum, progeria infantilis, senilism syndrome Associated persons: Jean-Martin Charcot Hastings Gilford Sir Jonathan Hutchinson Alexandre-Achille Souques Description: A very rare disease of premature aging in young children, characterized mainly by a birdlike, “wizened old man” facial appearance, premature bodily aging (progeria) and dwarfism. The children have large skulls, bird-like features, atrophy of muscles and skin, loss of subcutaneous fat, high serum lipid levels and early atherosclerotic changes in the vessels. The child is normal at birth. Intelligence is usually normal. The average age of death is 16 years, but survivors until 26 years have been recorded. Occur in children of both sexes. Death is usually caused by the effects of arteriosclerosis. Etiology and mode of genetic transmission (if any) is unknown. Hutchinson-Gilford progeria was discovered in 1886 by Jonathan Hutchinson. He documented the clinical features of a boy aged 6 years who had congenital absence of the hair and atrophy of the skin. Hastings Gilford followed up this patient and another, and in 1897 recognized it as a clinical entity and introduced the term “progeria” from the Greek work meaning “prematurely old.” In his case report published in 1904 he provided a set of pictures of the disorder from infancy to the age of 17 years, in which the characteristic alopecia, fat loss and premature aging are clearly depicted.

19. Telefacts -- The Site Telefacts reportage van de Vlaamse Televisie Maatschappij gewijd aan de aandoening progeria, inclusief dossier. http://www.vtm.be/telefacts/details.htm?id=20121

20. Progeria / The Family Village progeria Also known as HutchinsonGilford progeria Syndrome http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

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