{"version":"1.0","provider_name":"RARE DISEASE FOUNDATION","provider_url":"https:\/\/www.rarediseases.lt\/en\/","title":"Changes in epidermolysis bullosa treatment - RARE DISEASE FOUNDATION","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"uUWacHRZ5P\"><a href=\"https:\/\/www.rarediseases.lt\/en\/changes-in-epidermolysis-bullosa-treatment\/\">Changes in epidermolysis bullosa treatment<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.rarediseases.lt\/en\/changes-in-epidermolysis-bullosa-treatment\/embed\/#?secret=uUWacHRZ5P\" width=\"600\" height=\"338\" title=\"&#8220;Changes in epidermolysis bullosa treatment&#8221; &#8212; RARE DISEASE FOUNDATION\" data-secret=\"uUWacHRZ5P\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script>\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\/\/# sourceURL=https:\/\/www.rarediseases.lt\/lib\/js\/wp-embed.min.js' defer='defer\n<\/script>\n","thumbnail_url":"https:\/\/www.rarediseases.lt\/storage\/2017\/01\/rarediseases.lt_14407845_1317019421650854_695896060_o-002.jpg","thumbnail_width":2048,"thumbnail_height":2048,"description":"Coordinating Centre for Children\u2019s Rare Diseases together with Dermatovenerology Centre of Vilnius University Hospital Santariskiu Klinikos have prepared Epidermolysis bullosa diagnostics and treatment protocol. This protocol will facilitate patient care and acquisition of needed medicines and supplies for children affected with Epidermolysis bullosa. &nbsp; Epidermolysis bullosa is a group of rare hereditary diseases, which manifest [&hellip;]"}