{"id":21125,"date":"2025-11-17T01:45:41","date_gmt":"2025-11-16T22:45:41","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/marfan\/"},"modified":"2025-11-17T01:45:41","modified_gmt":"2025-11-16T22:45:41","slug":"marfan","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/marfan\/","title":{"rendered":"Marfan Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Marfan syndrome is an inherited disease that affects connective tissue.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Tall<\/li>\n<li>Arachnodactyly<\/li>\n<li>Lens dislocation<\/li>\n<li>Aortic aneurysm<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>FBN1 gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Clinical criteria, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Beta blockers, surgery.<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Genetics Polyclinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In case of suspicion of aortic dissection, emergency department should be consulted.<\/p>\n<p><em>This page is for general information purposes only.<\/em><\/p>","protected":false},"excerpt":{"rendered":"<p>Definition: Marfan syndrome is a hereditary disease affecting connective tissue. Symptoms: Tall stature, arachnodactyly, lens dislocation, aortic aneurysm. Causes: FBN1 gene mutation. Diagnosis: Clinical criteria, genetic testing. Treatment: Beta-blockers, surgery. Which Clinic Should You Go To? Genetics Clinic. What to Do in an Emergency? In case of suspected aortic dissection, go to the emergency room. This page is for general information purposes only.<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Marfan Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Marfan syndrome is a hereditary disorder affecting connective tissue. Symptoms: Tall stature, arachnodactyly, lens dislocation, aortic aneurysm. Causes: FBN1 gene"},"footnotes":""},"class_list":["post-21125","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21125","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\/21125\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21125"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}