1.0RARE DISEASE FOUNDATIONhttps://www.rarediseases.lt/en/rich600338<blockquote class="wp-embedded-content" data-secret="3sEvgsgDMH"><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=3sEvgsgDMH" width="600" height="338" title="“Changes in epidermolysis bullosa treatment” — RARE DISEASE FOUNDATION" data-secret="3sEvgsgDMH" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script type="text/javascript"> /*! This file is auto-generated */ !function(c,d){"use strict";var e=!1,o=!1;if(d.querySelector)if(c.addEventListener)e=!0;if(c.wp=c.wp||{},c.wp.receiveEmbedMessage);else if(c.wp.receiveEmbedMessage=function(e){var t=e.data;if(!t);else if(!(t.secret||t.message||t.value));else if(/[^a-zA-Z0-9]/.test(t.secret));else{for(var r,s,a,i=d.querySelectorAll('iframe[data-secret="'+t.secret+'"]'),n=d.querySelectorAll('blockquote[data-secret="'+t.secret+'"]'),o=new RegExp("^https?:$","i"),l=0;l<n.length;l++)n[l].style.display="none";for(l=0;l<i.length;l++)if(r=i[l],e.source!==r.contentWindow);else{if(r.removeAttribute("style"),"height"===t.message){if(1e3<(s=parseInt(t.value,10)))s=1e3;else if(~~s<200)s=200;r.height=s}if("link"===t.message)if(s=d.createElement("a"),a=d.createElement("a"),s.href=r.getAttribute("src"),a.href=t.value,!o.test(a.protocol));else if(a.host===s.host)if(d.activeElement===r)c.top.location.href=t.value}}},e)c.addEventListener("message",c.wp.receiveEmbedMessage,!1),d.addEventListener("DOMContentLoaded",t,!1),c.addEventListener("load",t,!1);function t(){if(o);else{o=!0;for(var e,t,r,s=-1!==navigator.appVersion.indexOf("MSIE 10"),a=!!navigator.userAgent.match(/Trident.*rv:11\./),i=d.querySelectorAll("iframe.wp-embedded-content"),n=0;n<i.length;n++){if(!(r=(t=i[n]).getAttribute("data-secret")))r=Math.random().toString(36).substr(2,10),t.src+="#?secret="+r,t.setAttribute("data-secret",r);if(s||a)(e=t.cloneNode(!0)).removeAttribute("security"),t.parentNode.replaceChild(e,t);t.contentWindow.postMessage({message:"ready",secret:r},"*")}}}}(window,document); </script> https://www.rarediseases.lt/storage/2017/01/rarediseases.lt_14407845_1317019421650854_695896060_o-002.jpg20482048Coordinating Centre for Children’s 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.   Epidermolysis bullosa is a group of rare hereditary diseases, which manifest […]