{"id":21082,"date":"2025-11-17T01:45:44","date_gmt":"2025-11-16T22:45:44","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/fenilketonuri\/"},"modified":"2025-11-17T01:45:44","modified_gmt":"2025-11-16T22:45:44","slug":"fenilketonuri","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/fenilketonuri\/","title":{"rendered":"Phenylketonuria"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Phenylketonuria is a metabolic disease characterized by phenylalanine hydroxylase enzyme deficiency, accompanied by mental retardation and neurological disorders.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Mental retardation<\/li>\n<li>Neurological disorder<\/li>\n<li>Hypopigmentation<\/li>\n<li>Eczematous rash<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>PAH gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Newborn screening, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Low phenylalanine diet.<\/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 metabolic crisis, 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: Phenylketonuria (PAH) is a metabolic disease characterized by phenylalanine hydroxylase enzyme deficiency, resulting in mental retardation and neurological impairment. Symptoms: Mental retardation, neurological impairment, hypopigmentation, eczematous rash. Causes: PAH gene mutation. Diagnosis: Newborn screening, genetic testing. Treatment: Low phenylalanine diet. Which Clinic Should You Go To? Metabolism Clinic. What to Do in an Emergency? In case of a metabolic crisis, you should go to the emergency room. This [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Phenylketonuria - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Phenylketonuria (PKU) is a metabolic disorder characterized by a deficiency in the phenylalanine hydroxylase enzyme, resulting in mental retardation and neurological impairment."},"footnotes":""},"class_list":["post-21082","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21082","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\/21082\/revisions"}],"predecessor-version":[{"id":21282,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21082\/revisions\/21282"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21082"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}