{"id":3475,"date":"2024-12-10T09:34:38","date_gmt":"2024-12-10T16:34:38","guid":{"rendered":"http:\/\/liver.ca\/?page_id=3475"},"modified":"2025-01-09T13:53:20","modified_gmt":"2025-01-09T20:53:20","slug":"tyrosinemie","status":"publish","type":"page","link":"https:\/\/liver.ca\/fr\/tyrosinemia\/","title":{"rendered":"Tyrosin\u00e9mie"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":4,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"templates\/liver-disease.php","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-3475","page","type-page","status-publish","hentry"],"acf":{"title":"","text":"Tyrosinemia is a rare genetic metabolic disorder characterized by the inability to break down the amino acid tyrosine due to a deficiency of the enzyme fumarylacetoacetate hydrolase (FAH). In families where both parents are carriers of the gene for the disease, there is a one in four risk that a child will have tyrosinemia.","image":4163,"landing_page":false,"story":"","bg_colour":"none","story_pretitle":"","story_title":"","story_text":"","story_image":""},"_links":{"self":[{"href":"https:\/\/liver.ca\/fr\/wp-json\/wp\/v2\/pages\/3475","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/liver.ca\/fr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/liver.ca\/fr\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/liver.ca\/fr\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/liver.ca\/fr\/wp-json\/wp\/v2\/comments?post=3475"}],"version-history":[{"count":0,"href":"https:\/\/liver.ca\/fr\/wp-json\/wp\/v2\/pages\/3475\/revisions"}],"wp:attachment":[{"href":"https:\/\/liver.ca\/fr\/wp-json\/wp\/v2\/media?parent=3475"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}