{"version":"1.0","provider_name":"Geneetika ja personaalmeditsiini kliinik","provider_url":"https:\/\/www.kliinikum.ee\/geneetika","author_name":"K\u00fclli Kevv\u00e4i","author_url":"https:\/\/www.kliinikum.ee\/geneetika\/author\/kyllikev\/","title":"Rasedate n\u00f5ustamine ja s\u00fcnnieelne diagnostika - Geneetika ja personaalmeditsiini kliinik","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"OeWSwM9VDi\"><a href=\"https:\/\/www.kliinikum.ee\/geneetika\/infomaterjalid-2\/sunnieelne-diagnostika\/\">Rasedate n\u00f5ustamine ja s\u00fcnnieelne diagnostika<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.kliinikum.ee\/geneetika\/infomaterjalid-2\/sunnieelne-diagnostika\/embed\/#?secret=OeWSwM9VDi\" width=\"600\" height=\"338\" title=\"&#8220;Rasedate n\u00f5ustamine ja s\u00fcnnieelne diagnostika&#8221; &#8212; Geneetika ja personaalmeditsiini kliinik\" data-secret=\"OeWSwM9VDi\" 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.kliinikum.ee\/geneetika\/wp-includes\/js\/wp-embed.min.js\n<\/script>\n","description":"S\u00fcnnieelne diagnostika S\u00fcnnieelne diagnostika v\u00f5imaldab juba \u00fcsasiseselt diagnoosida mitmesuguseid p\u00e4rilikke haigusi ja seega m\u00e4\u00e4rata, kas oodatav laps on antud haiguse suhtes terve v\u00f5i mitte. Kasutatakse mitmesuguseid mitteinvasiivseid (ultraheliuuring) ja invasiivseid meetodeid (amniotsentees, koorioni biopsia).&nbsp; M\u00f5nda uuringut pakutakse k\u00f5ikidele rasedatele (s\u00f5eluuringud ehk skriiningud), teisi soovitatakse vaid neile, kellel on k\u00f5rgenenud risk kromosoomihaigusega lapse s\u00fcnniks (loote kromosoomianal\u00fc\u00fcs). [&hellip;]"}