{"id":21162,"date":"2025-11-17T01:45:41","date_gmt":"2025-11-16T22:45:41","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/apert\/"},"modified":"2025-11-17T01:45:41","modified_gmt":"2025-11-16T22:45:41","slug":"apert","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/apert\/","title":{"rendered":"Apert Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Apert syndrome is a congenital syndrome characterized by craniosynostosis, facial hypoplasia and syndactyly.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Craniosynostosis<\/li>\n<li>Facial hypoplasia<\/li>\n<li>Syndactyly<\/li>\n<li>Developmental delay<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>FGFR2 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 increased cranial pressure, 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: Apert syndrome is a congenital syndrome characterized by craniosynostosis, facial hypoplasia, and syndactyly. Symptoms: Craniosynostosis, Facial hypoplasia, Syndactyly, Developmental delay. Causes: FGFR2 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 increased cranial pressure, 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":"Apert Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Apert syndrome is a congenital syndrome characterized by craniosynostosis, facial hypoplasia, and syndactyly. Symptoms: Craniosynostosis, Facial hypoplasia, Syndactyly"},"footnotes":""},"class_list":["post-21162","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21162","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\/21162\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21162"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}