{"version":"1.0","provider_name":"CUTIS LAXA INTERNATIONALE","provider_url":"https:\/\/www.cutislaxa.org\/fr\/","title":"4\u00e8me Plan National Maladies rares en France - CUTIS LAXA INTERNATIONALE","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"A3M9PHT8LV\"><a href=\"https:\/\/www.cutislaxa.org\/fr\/4eme-plan-national-maladies-rares-en-france\/\">4\u00e8me Plan National Maladies rares en France<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.cutislaxa.org\/fr\/4eme-plan-national-maladies-rares-en-france\/embed\/#?secret=A3M9PHT8LV\" width=\"600\" height=\"338\" title=\"\u00ab\u00a04\u00e8me Plan National Maladies rares en France\u00a0\u00bb &#8212; CUTIS LAXA INTERNATIONALE\" data-secret=\"A3M9PHT8LV\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script type=\"text\/javascript\">\n\/* <![CDATA[ *\/\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/* ]]> *\/\n<\/script>\n","thumbnail_url":"https:\/\/www.cutislaxa.org\/wp-content\/uploads\/2020\/02\/France.jpg","thumbnail_width":225,"thumbnail_height":225,"description":"Le 25 F\u00e9vrier, le 4\u00e8me Plan National Maladies Rares a enfin \u00e9t\u00e9 lanc\u00e9 en France. Attendu depuis longtemps, mais retard\u00e9 par le contexte politique, il vise \u00e0 \u00e9largir et \u00e0 poursuivre le travail accompli par les pr\u00e9c\u00e9dents Plans. Il s\u2019articule autour de 4 axes\u00a0: Am\u00e9liorer le parcours de vie et de soin (renforcer les liens [&hellip;]"}