{"id":21161,"date":"2025-11-17T01:45:41","date_gmt":"2025-11-16T22:45:41","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/treacher-collins\/"},"modified":"2025-11-17T01:45:41","modified_gmt":"2025-11-16T22:45:41","slug":"treacher-collins","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/treacher-collins\/","title":{"rendered":"Treacher Collins Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Treacher Collins syndrome is a congenital syndrome characterized by hypoplasia of the facial bones.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Malar hypoplasia<\/li>\n<li>Lower eyelid coloboma<\/li>\n<li>Microtia<\/li>\n<li>Hearing loss<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>TCOF1 gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Clinical findings, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Surgical reconstruction.<\/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 respiratory distress, 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: Treacher-Collins syndrome is a congenital syndrome characterized by hypoplasia of the facial bones. Symptoms: Malar hypoplasia, lower eyelid coloboma, microtia, hearing loss. Causes: TCOF1 gene mutation. Diagnosis: Clinical findings, genetic testing. Treatment: Surgical reconstruction. Which Clinic Should You Go To? Genetics Clinic. What to Do in an Emergency? In case of respiratory distress, 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":"Treacher Collins Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Treacher-Collins syndrome is a congenital syndrome characterized by hypoplasia of the facial bones. Symptoms: Malar hypoplasia, lower eyelid coloboma, microscopic"},"footnotes":""},"class_list":["post-21161","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21161","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\/21161\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21161"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}