{"version":"1.0","provider_name":"Geenidiagnostiikka","provider_url":"https:\/\/sites.uef.fi\/genediagnostics","title":"APECED - Geenidiagnostiikka","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"7hq5OuJQkw\"><a href=\"https:\/\/sites.uef.fi\/genediagnostics\/monogeeniset-sairaudet\/apeced\/\">APECED<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/sites.uef.fi\/genediagnostics\/monogeeniset-sairaudet\/apeced\/embed\/#?secret=7hq5OuJQkw\" width=\"600\" height=\"338\" title=\"&#8221;APECED&#8221; &#8212; Geenidiagnostiikka\" data-secret=\"7hq5OuJQkw\" 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\/\/# sourceURL=https:\/\/sites.uef.fi\/genediagnostics\/wp-includes\/js\/wp-embed.min.js\n\/* ]]> *\/\n<\/script>\n","thumbnail_url":"https:\/\/sites.uef.fi\/genediagnostics\/wp-content\/uploads\/sites\/100\/2020\/06\/T321_cmyk_15189-3-e1593515084545.jpg","thumbnail_width":169,"thumbnail_height":107,"description":"Tyypin 1 APECED (autoimmuunipolyendokrinopatia-kandidiaasi-ektodermidystrofia, ORPHA 3453, OMIM 240300) on suomalaiseen tautiperint\u00f6\u00f6n liittyv\u00e4 sairaus, joka periytyy autosomissa resessiivisesti. Sairaus on varsin harvinainen, sill\u00e4 vuosittain syntyy keskim\u00e4\u00e4rin kaksi lasta, joilla on APECED. Tuhannesta suomalaisesta keskim\u00e4\u00e4rin 5\u201310 (0,5\u20131 %) on viallisen APECED-geenin kantajia. Taudin erilaiset elinspesifiset autoimmuunitautien ilmentym\u00e4t ovat: suun hiivasieni tai muu hiivatulehdus, lis\u00e4kilpirauhasen vajaatoiminta, lis\u00e4munuaiskuoren vajaatoiminta, [&hellip;]"}