{"id":21349,"date":"2025-11-17T01:45:46","date_gmt":"2025-11-16T22:45:46","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/cockayne-sendromu\/"},"modified":"2025-11-17T01:45:46","modified_gmt":"2025-11-16T22:45:46","slug":"cockayne-sendromu","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/cockayne-sendromu\/","title":{"rendered":"Cockayne Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Cockayne syndrome is a rare autosomal recessive genetic disorder characterized by microcephaly, growth retardation, neurological disorders, and photosensitivity.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Microcephaly<\/li>\n<li>Developmental delay<\/li>\n<li>Neurological decline<\/li>\n<li>Eye anomalies<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>Mutation in the ERCC6 or ERCC8 genes.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Clinical findings, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Symptomatic and supportive treatment.<\/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 seizure, 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 Cockayne syndrome is a rare autosomal recessive genetic disorder characterized by microcephaly, growth retardation, neurological disorders, and photosensitivity. Symptoms Microcephaly Growth retardation Neurological regression Eye abnormalities Causes Mutation in the ERCC6 or ERCC8 genes. Diagnosis Clinical findings, genetic testing. Treatment Symptomatic and supportive treatment. Which Clinic Should You Go To? Genetics Clinic What to Do in an Emergency? In case of a seizure, emergency [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Cockayne Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Cockayne syndrome is a rare, autosomal recessive genetic disorder characterized by microcephaly, growth retardation, neurological disorders, and photosensitivity."},"footnotes":""},"class_list":["post-21349","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21349","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\/21349\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21349"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}