{"id":21347,"date":"2025-11-17T01:45:46","date_gmt":"2025-11-16T22:45:46","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/werner-sendromu\/"},"modified":"2025-11-17T01:45:46","modified_gmt":"2025-11-16T22:45:46","slug":"werner-sendromu","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/werner-sendromu\/","title":{"rendered":"Werner Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Werner syndrome is an autosomal recessive progeroid syndrome characterized by premature aging, cataracts, skin changes, and a predisposition to cancer.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Signs of premature aging<\/li>\n<li>Cataracts at a young age<\/li>\n<li>Scleroderma-like skin changes<\/li>\n<li>Increased risk of cancer<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>Mutation in the WRN gene.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Clinical criteria, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Symptomatic treatment, cancer screening.<\/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 acute myocardial infarction, 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 Werner syndrome is an autosomal recessive progeroid syndrome characterized by premature aging, cataracts, skin changes, and a predisposition to cancer. Symptoms Signs of premature aging Cataracts at a young age Scleroderma-like skin changes Increased cancer risk Causes Mutation in the WRN gene. Diagnosis Clinical criteria, genetic testing. Treatment Symptomatic treatment, cancer screening. Which Clinic Should You Visit? Genetics Clinic What to Do in an Emergency [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Werner Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Werner syndrome is an autosomal recessive progeroid syndrome characterized by premature aging, cataracts, skin changes, and a predisposition to cancer. Symptoms"},"footnotes":""},"class_list":["post-21347","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21347","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\/21347\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21347"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}