1.0PTC Therapeutics (Italy)https://panel.ptcbio.com/it-p2025tcrich600338<blockquote class="wp-embedded-content" data-secret="HA8qkOI4hE"><a href="https://panel.ptcbio.com/it-p2025tc/therapeutic-areas/familial-chylomicronemia-syndrome/">Familial chylomicronemia syndrome</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://panel.ptcbio.com/it-p2025tc/therapeutic-areas/familial-chylomicronemia-syndrome/embed/#?secret=HA8qkOI4hE" width="600" height="338" title="“Familial chylomicronemia syndrome” — PTC Therapeutics (Italy)" data-secret="HA8qkOI4hE" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script type="text/javascript"> /* <![CDATA[ */ /*! This file is auto-generated */ !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); //# sourceURL=https://panel.ptcbio.com/it-p2025tc/wp-includes/js/wp-embed.min.js /* ]]> */ </script> What is Familial Chylomicronemia Syndrome? Familial Chylomicronemia Syndrome (FCS) is a rare genetic and hereditary disease that prevents the body from digesting fats (triglycerides)1, leaving the patient debilitated and, depending on the severity, leading to death. FCS can manifest at various points in life, from childhood to adulthood.​ ​The signs and symptoms of FCS include2:​…https://panel.ptcbio.com/it-p2025tc/wp-content/uploads/sites/21/2024/12/FCS-Signs-and-Symptoms-scaled-1.jpg