{"version":"1.0","provider_name":"Geenidiagnostiikka","provider_url":"https:\/\/sites.uef.fi\/genediagnostics","title":"Sitosterolemia - Geenidiagnostiikka","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"fLa3kbq3PM\"><a href=\"https:\/\/sites.uef.fi\/genediagnostics\/monogeeniset-sairaudet\/sitosterolemia\/\">Sitosterolemia<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/sites.uef.fi\/genediagnostics\/monogeeniset-sairaudet\/sitosterolemia\/embed\/#?secret=fLa3kbq3PM\" width=\"600\" height=\"338\" title=\"&#8221;Sitosterolemia&#8221; &#8212; Geenidiagnostiikka\" data-secret=\"fLa3kbq3PM\" 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":"Sitosterolemian (Tyyppi 1 OMIM 210250 ja tyyppi 2 OMIM 618666) aiheuttavat geenivirheet\u00a0ABCG5&#8211; ja\u00a0ABCG8\u00a0-geeneiss\u00e4, mitk\u00e4 sijaitsevat kromosomissa 2p21. Sitosterolemia on autosomissa resistentist\u00ed periytyv\u00e4 harvinainen sairaus, joka johtaa kasvisitosterolien ja kolesterolin kasautumiseen elimist\u00f6\u00f6n ja varhaiseen sepelvaltiomotautiin. Tauti kuvattiin ensimm\u00e4isen kerran 1974. Suomessa tautitapauksia on kuvattu vain muutamia. ABCG5 ja ABCG8 sijaitsevat enterosyyttien ja maksasolujen apikaalisella pinnalla, miss\u00e4 [&hellip;]"}