{"id":21150,"date":"2025-11-17T01:45:45","date_gmt":"2025-11-16T22:45:45","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/carney\/"},"modified":"2025-11-17T01:45:45","modified_gmt":"2025-11-16T22:45:45","slug":"carney-kompleksi","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/carney-kompleksi\/","title":{"rendered":"Carney Complex"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Carney complex is a rare autosomal dominant genetic syndrome characterized by multiple myxomas, skin pigmentation, and various endocrine tumors.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Cardiac myxomas<\/li>\n<li>Lentigines and bluish nevi on the skin<\/li>\n<li>Primary pigmented nodular adrenal disease (PPNAD)<\/li>\n<li>Pituitary adenomas<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>Inactivating mutation in the PRKAR1A gene.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Clinical criteria, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Surgery for tumors, regular screening.<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Endocrinology Polyclinic<\/strong> or <strong>Genetics Polyclinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In case of signs of embolism or obstruction due to cardiac myxoma, emergency department should be consulted.<\/p>\n<p><em>This page is for general information purposes only.<\/em><\/p>","protected":false},"excerpt":{"rendered":"<p>Definition: Carney complex is a rare autosomal dominant genetic syndrome characterized by multiple myxomas, skin pigmentation, and various endocrine tumors. Symptoms: Cardiac myxomas, Lentigines and bluish nevi on the skin, Primary pigmented nodular adrenal disease (PPNAD), Pituitary adenomas. Causes: Inactivating mutation in the PRKAR1A gene. Diagnosis: Clinical criteria, genetic testing. Treatment: Surgery targeting tumors, regular screening. Which Clinic Should You Consult? [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Carney Complex - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Carney complex is a rare genetic syndrome with autosomal dominant inheritance, characterized by multiple myxomas, skin pigmentation, and various endocrine tumors."},"footnotes":""},"class_list":["post-21150","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21150","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":1,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21150\/revisions"}],"predecessor-version":[{"id":21327,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21150\/revisions\/21327"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21150"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}