{"version":"1.0","provider_name":"Retina Club","provider_url":"https:\/\/retinaclub.es\/en\/","author_name":"retina","author_url":"https:\/\/retinaclub.es\/en\/author\/retina\/","title":"Rod dystrophy secondary to PRPF31 mutation - Retina Club","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"JA1Ec3JQa2\"><a href=\"https:\/\/retinaclub.es\/en\/caso\/rod-dystrophy-secondary-to-prpf31-mutation\/\">Rod dystrophy secondary to PRPF31 mutation<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/retinaclub.es\/en\/caso\/rod-dystrophy-secondary-to-prpf31-mutation\/embed\/#?secret=JA1Ec3JQa2\" width=\"600\" height=\"338\" title=\"&#8220;Rod dystrophy secondary to PRPF31 mutation&#8221; &#8212; Retina Club\" data-secret=\"JA1Ec3JQa2\" 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:\/\/retinaclub.es\/wp-includes\/js\/wp-embed.min.js\n\/* ]]> *\/\n<\/script>\n","thumbnail_url":"https:\/\/retinaclub.es\/wp-content\/uploads\/2024\/09\/A-copia-35.webp","thumbnail_width":989,"thumbnail_height":991,"description":"Retinitis pigmentosa (also known as rod dystrophy) encompasses a group of clinically and genetically heterogeneous hereditary retinal disorders. It is characterized by progressive dysfunction of the retinal pigment epithelium and photoreceptors, affecting rods first and cones later. It usually manifests as difficulty with night vision and reduction of peripheral visual field, starting in adolescence. The [&hellip;]"}