{"id":21224,"date":"2025-11-17T01:45:42","date_gmt":"2025-11-16T22:45:42","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/stickler\/"},"modified":"2025-11-17T01:45:42","modified_gmt":"2025-11-16T22:45:42","slug":"stickler","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/stickler\/","title":{"rendered":"Stickler Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Stickler syndrome is an inherited connective tissue disease characterized by myopia, risk of retinal detachment, and facial anomalies.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Myopia<\/li>\n<li>Risk of retinal detachment<\/li>\n<li>Cleft palate<\/li>\n<li>Hearing loss<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>COL2A1, COL11A1 gene mutations.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Clinical findings, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Ophthalmological follow-up.<\/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 retinal detachment, 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 Stickler syndrome is a hereditary connective tissue disorder characterized by myopia, risk of retinal detachment, and facial anomalies. Symptoms Myopia Risk of retinal detachment Cleft palate Hearing loss Causes COL2A1, COL11A1 gene mutations. Diagnosis Clinical findings, genetic testing. Treatment Ophthalmological follow-up. Which Clinic Should You Go To? Genetics Clinic What to Do in an Emergency? In case of suspected retinal detachment, go to the emergency room. [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Stickler Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Stickler syndrome is a hereditary connective tissue disorder characterized by myopia, risk of retinal detachment, and facial anomalies. Symptoms: Myopia, Retinal detachment"},"footnotes":""},"class_list":["post-21224","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21224","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\/21224\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21224"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}