{"id":21183,"date":"2025-11-17T01:45:42","date_gmt":"2025-11-16T22:45:42","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/cornelia-de-lange\/"},"modified":"2025-11-17T01:45:42","modified_gmt":"2025-11-16T22:45:42","slug":"cornelia-de-lange","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/cornelia-de-lange\/","title":{"rendered":"Cornelia de Lange Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Cornelia de Lange syndrome is a hereditary disorder characterized by developmental delay, characteristic facial appearance, and upper extremity anomalies.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Developmental delay<\/li>\n<li>Characteristic face<\/li>\n<li>Microcephaly<\/li>\n<li>Upper extremity anomalies<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>NIPBL or other gene mutations.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Clinical findings, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Symptomatic 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 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 Cornelia de Lange syndrome is a hereditary disorder characterized by developmental delay, a characteristic facial feature, and upper extremity anomalies. Symptoms Developmental delay Characteristic facial features Microcephaly Upper extremity anomalies Causes NIPBL or other gene mutations. Diagnosis Clinical findings, genetic testing. Treatment Symptomatic treatment. Which Clinic Should You Go To? Genetics Clinic What to Do in an Emergency? In case of respiratory distress, seek emergency care [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Cornelia de Lange Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Cornelia de Lange syndrome is a hereditary disorder characterized by developmental delay, a characteristic facial feature, and upper extremity anomalies. Symptoms"},"footnotes":""},"class_list":["post-21183","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21183","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\/21183\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21183"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}