progeria-france.blogspot.com
Progeria Family Circle: Les symptômes
http://progeria-france.blogspot.com/p/les-symptomes.html
Les symptômes et le diagnostic. Le développement intellectuel et émotionnel des enfants atteints de la progéria est normal. Cependant, durant la 1ère année de leur vie, ces enfants commencent à développer des atteintes physiques. La croissance est ralentie, leurs cheveux commencent à tomber et ils perdent la graisse sous-cutanée. Dans l’étude de Hennekam de 2006 ( 1. L’âge moyen du diagnostic de 72 patients HGPS était de 2.9 années. Il est important de faire ses études de comparaison des patients HGPS au...
progeria-france.blogspot.com
Progeria Family Circle: janvier 2015
http://progeria-france.blogspot.com/2015_01_01_archive.html
Les chercheurs, les parents et les patients se sont rencontrés à Marseille. Le 16 janvier dernier les chercheurs italiens et français qui étudient les laminopathies se sont rencontrés à Marseille. C'était une réunion combinée pour médecins et patients, incluant également les parents des enfants progéria. Les laminopathies comprennent toutes les maladies, incluant la progéria, causées par un fonctionnement anormal du gène LMNA qui produit les lamines A et C. L'utilité d'utiliser d'autres médicaments reste...
progeria-france.blogspot.com
Progeria Family Circle: une étude espagnole donne de l’espoir pour une thérapie pour la progéria et le cancer
http://progeria-france.blogspot.com/2014/11/une-etude-espagnole-donne-de-lespoir.html
Une étude espagnole donne de l’espoir pour une thérapie pour la progéria et le cancer. Pour mener leur étude. Un des chercheurs de cette étude, constate que ces résultats sont très encourageants d’un point de vue scientifique mais il reste prudent sur les avancées vers des applications thérapeutiques. José Maria Pérez Freije. Publié par Marjet Stamsnijder. Inscription à : Publier les commentaires (Atom). Depuis 1997, nous avons offert:. Le soutien aux familles individuelles. Michiel and Amber - BE. Une é...
progeria-france.blogspot.com
Progeria Family Circle: Joyeuses Fêtes!
http://progeria-france.blogspot.com/2014/12/joyeuses-fetes.html
Publié par Marjet Stamsnijder. Inscription à : Publier les commentaires (Atom). Le cercle de la famille de progeria est du réseau qui soutient les enfants progeria européennes et leurs familles. Depuis 1997, nous avons offert:. Le soutien aux familles individuelles. Mises à informations actualisées. Prise de conscience accrue de l'acceptation du public. Le soutien aux soins médicaux et de la recherche. Contactez-nous à: info@progeria.nu. Michiel and Amber - BE. Micael Correia - FR, PT, EN, NL, IT.
progeriafamilycircle.blogspot.com
progeria family circle: cause
http://progeriafamilycircle.blogspot.com/p/cause.html
How you can help. The French Dr. Nicolas Lévy discovered in a Progeria patient the location of the gene defect on the DNA. This discovery, done in 2003, was independently confirmed by American scientists. Progeria is caused by a genetic defect in. In Figure 1 below, it can be seen that the LMNA gene is found at the location 1q21.2. Its location is marked by the yellow arrow. Each chromosome has a p and a q arm. P (Petit = small) is the short arm, and q (the next letter in the alphabet) is...On chromosome...
progeriafamilycircle.blogspot.com
progeria family circle: special... with good reason
http://progeriafamilycircle.blogspot.com/2013/11/special-with-good-reason.html
How you can help. Special. with good reason. In this documentary three members of the progeria family circle 'dreamteam' explain why they help to bring the progeria children and their families together. Posted by Marjet Stamsnijder. Subscribe to: Post Comments (Atom). Find us on facebook. The progeria Family Circle is a parents network that supports European Progeria children and their families. Since 1997 we have offered:. Support for individual families. Raised awareness for public acceptance.
progeriafamilycircle.blogspot.com
progeria family circle: Progeria Reunion and Scientific Workshop
http://progeriafamilycircle.blogspot.com/2012/10/scientific-meeting.html
How you can help. Progeria Reunion and Scientific Workshop. In september 2012 scientific researchers from all over the world met in Italy to share the results of their search for a treatment for progeria children. This congress was organised by Giovanna Lantanzi and Stefano Squarzoni form the University of Bologna, and made possible through donations of the Italian organisation for children with progeria: A.I. Pro Sammy Basso. Another approach is the antisense therapy, with a morpholino. Annachiara D...
progeriafamilycircle.blogspot.com
progeria family circle: The Big Run: 10 Marathons in 10 days
http://progeriafamilycircle.blogspot.com/2012/03/big-run.html
How you can help. The Big Run: 10 Marathons in 10 days. Charlotte Okines and Becky Reid are planning a sponsor run for the Progeria Family Circle. The route goes from Yorkshire to Kent. They will run 10 marathons in 10 days! Starting on April 5th, they hope to finish their 438 km long run on 14th of April 2012. Charlotte and her friend Becky will start in Yorkshire, because Harry – another Progeria sufferer and close friend of Charlotte’s sister Hayley – lives there. They will then ...Find us on facebook.
progeriafamilycircle.blogspot.com
progeria family circle: symptoms
http://progeriafamilycircle.blogspot.com/p/symptoms.html
How you can help. Children with Progeria go through normal intellectual and emotional development. During their first years of life, however, it becomes increasingly clear that their physical development does not run its normal course. Growth stagnates, the hair starts to fall out, and they lose subcutaneous fat. Development and course of Classic Progeria. Meanwhile, the children’s psychosocial and intellectual developments proceed normally. Their speaking ability is generally good, but they ha...The mos...
progeriafamilycircle.blogspot.com
progeria family circle: progeria
http://progeriafamilycircle.blogspot.com/p/hutchinson-gilford-progeria-syndrome.html
How you can help. Progeria is a very rare disease. Currently, there are approximately 100 known Progeria-patients worldwide. It is for this reason that only few doctors have encountered the syndrome in medical practice. In Europe, we know of approximately 30 children with (a form of) Progeria. The disease is found everywhere in the world, regardless of race or skin colour. It occurs almost equally among boys and girls. There is an extremely rare possibility of a Progeria child getting a little br...The c...
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