{"version":"1.0","provider_name":"Geenidiagnostiikka","provider_url":"https:\/\/sites.uef.fi\/genediagnostics","title":"Monogeeninen diabetes - Geenidiagnostiikka","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"cIcvGJLcR0\"><a href=\"https:\/\/sites.uef.fi\/genediagnostics\/monogeeniset-sairaudet\/monogeeninen-diabetes\/\">Monogeeninen diabetes<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/sites.uef.fi\/genediagnostics\/monogeeniset-sairaudet\/monogeeninen-diabetes\/embed\/#?secret=cIcvGJLcR0\" width=\"600\" height=\"338\" title=\"&#8221;Monogeeninen diabetes&#8221; &#8212; Geenidiagnostiikka\" data-secret=\"cIcvGJLcR0\" 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":"Monogeenisi\u00e4 eli yhden geenimuutoksen aiheuttamia diabetesmuotoja ovat varhaisessa imev\u00e4isi\u00e4ss\u00e4 puhkeava diabetes (PNDM, Permanent Neonatal Diabetes Mellitus), MODY-tyypin diabetes (Maturity-Onset Diabetes of the Young) ja mitokondriaalinen diabetes. Etenkin kahden ensimm\u00e4isen diabetesmuodon erottaminen toisistaan on joissakin tapauksissa haastavaa. T\u00e4m\u00e4n vuoksi olemme katsoneet tarpeelliseksi luoda palvelututkimuksen, jossa sekvensoimme kaikki tunnetut n\u00e4it\u00e4 kolmea diabetestyyppi\u00e4 aiheuttavat geenit, ja teemme my\u00f6s [&hellip;]"}