1.0PIAM farmaceutici s.p.ahttps://www.piamfarmaceutici.com/en/morehttps://www.piamfarmaceutici.com/en/author/more/rich600338<blockquote class="wp-embedded-content" data-secret="Ln7dbJmNnN"><a href="https://www.piamfarmaceutici.com/en/patologia/homocystinuria-hom-2/">Homocystinuria (HOM)</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://www.piamfarmaceutici.com/en/patologia/homocystinuria-hom-2/embed/#?secret=Ln7dbJmNnN" width="600" height="338" title="“Homocystinuria (HOM)” — PIAM farmaceutici s.p.a" data-secret="Ln7dbJmNnN" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script> /*! 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://www.piamfarmaceutici.com/wp/wp-includes/js/wp-embed.min.js </script> https://www.piamfarmaceutici.com/wp-content/uploads/2023/01/homocistinuria-HOM-4.jpg19201280Classical homocystinuria is an inherited metabolic disease characterized by the deficiency of an enzyme involved in the methyl metabolic pathway of the amino acid methionine. This deficiency leads to the accumulation of the amino acid homocysteine ​​in the blood and urine. Amino acids are the constituent units of proteins and are therefore daily taken as […]