{"id":21272,"date":"2025-11-17T01:45:44","date_gmt":"2025-11-16T22:45:44","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/cpt-ii\/"},"modified":"2025-11-17T01:45:44","modified_gmt":"2025-11-16T22:45:44","slug":"cpt-ii","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/cpt-ii\/","title":{"rendered":"CPT II Deficiency"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>CPT II deficiency is a metabolic disease characterized by long-chain fatty acid oxidation defect and characterized by rhabdomyolysis and myoglobinuria.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Exercise intolerance<\/li>\n<li>Rhabdomyolysis<\/li>\n<li>Myoglobinuria<\/li>\n<li>Kidney failure<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>CPT2 gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Muscle biopsy, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Dietary modification, MCT oil.<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Metabolism Polyclinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In case of rhabdomyolysis, 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: CPT2 deficiency is a metabolic disease characterized by a long-chain fatty acid oxidation defect, resulting in rhabdomyolysis and myoglobinuria. Symptoms: Exercise intolerance, rhabdomyolysis, myoglobinuria, renal failure. Causes: CPT2 gene mutation. Diagnosis: Muscle biopsy, genetic testing. Treatment: Dietary modification, MCT oil. Which Clinic Should You Go To? Metabolism Clinic. What to Do in an Emergency? In case of rhabdomyolysis, 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":"CPT II Deficiency - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: CPT II deficiency is a metabolic disease characterized by a long-chain fatty acid oxidation defect, resulting in rhabdomyolysis and myoglobinuria. Symptoms"},"footnotes":""},"class_list":["post-21272","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21272","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\/21272\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21272"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}