{"id":21187,"date":"2025-11-17T01:45:42","date_gmt":"2025-11-16T22:45:42","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/kabuki\/"},"modified":"2025-11-17T01:45:42","modified_gmt":"2025-11-16T22:45:42","slug":"kabuki","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/kabuki\/","title":{"rendered":"Kabuki Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Kabuki syndrome is an inherited disorder characterized by characteristic facial appearance, developmental delay, and skeletal abnormalities.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Kabuki makeup face<\/li>\n<li>Developmental delay<\/li>\n<li>Short fingers<\/li>\n<li>Cardiac anomalies<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>KMT2D or KDM6A 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: Kabuki syndrome is a hereditary disorder characterized by a characteristic facial appearance, developmental delay, and skeletal anomalies. Symptoms: Kabuki makeup face, developmental delay, short fingers, cardiac anomalies. Causes: KMT2D or KDM6A 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, 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":"Kabuki Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Kabuki syndrome is a hereditary disorder characterized by a characteristic facial appearance, developmental delay, and skeletal anomalies. Symptoms: Kabuki makeup"},"footnotes":""},"class_list":["post-21187","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21187","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\/21187\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21187"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}