{"id":21118,"date":"2025-11-17T01:45:40","date_gmt":"2025-11-16T22:45:40","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/wilson\/"},"modified":"2025-11-17T01:45:40","modified_gmt":"2025-11-16T22:45:40","slug":"wilson","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/wilson\/","title":{"rendered":"Wilson&#039;s Disease"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Wilson&#039;s disease is an inherited disease characterized by copper accumulation in the liver and brain as a result of copper metabolism disorders.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Liver failure<\/li>\n<li>Neurological symptoms<\/li>\n<li>Kayser-Fleischer ring<\/li>\n<li>Psychiatric symptoms<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>ATP7B gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Ceruloplasmin, urine copper, liver biopsy.<\/p>\n<h2>Treatment<\/h2>\n<p>Penicillamine, zinc, liver transplantation.<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Gastroenterology Polyclinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In case of acute liver failure, emergency services should be consulted.<\/p>\n<p><em>This page is for general information purposes only.<\/em><\/p>","protected":false},"excerpt":{"rendered":"<p>Definition Wilson&#039;s disease is a hereditary disease characterized by copper accumulation in the liver and brain due to a disorder of copper metabolism. Symptoms Liver failure Neurological symptoms Kayser-Fleischer ring Psychiatric symptoms Causes ATP7B gene mutation. Diagnosis Ceruloplasmin, urinary copper, liver biopsy. Treatment Penicillamine, zinc, liver transplant. Which Clinic Should You Go To? Gastroenterology Clinic What to Do in an Emergency? In case of acute liver failure, emergency [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Wilson&#039;s Disease - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Wilson&#039;s disease is a hereditary disorder characterized by the accumulation of copper in the liver and brain due to a disorder of copper metabolism. Symptoms: Liver"},"footnotes":""},"class_list":["post-21118","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21118","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar"}],"about":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/types\/hastaliklar"}],"author":[{"embeddable":true,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/users\/1"}],"version-history":[{"count":0,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21118\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21118"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}