{"id":21250,"date":"2025-11-17T01:45:43","date_gmt":"2025-11-16T22:45:43","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/pompe\/"},"modified":"2025-11-17T01:45:43","modified_gmt":"2025-11-16T22:45:43","slug":"pompe","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/pompe\/","title":{"rendered":"Pompe Disease"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Pompe disease is a lysosomal storage disease characterized by progressive myopathy and cardiomyopathy, resulting from acid alpha-glucosidase enzyme deficiency.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Hypotonia<\/li>\n<li>Cardiomegaly<\/li>\n<li>Respiratory Failure<\/li>\n<li>Progressive muscle weakness<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>GAA gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Enzyme activity, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Enzyme replacement therapy.<\/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 respiratory failure, 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 Pompe disease is a lysosomal storage disease characterized by progressive myopathy and cardiomyopathy resulting from acid alpha-glucosidase enzyme deficiency. Symptoms Hypotonia Cardiomegaly Respiratory failure Progressive muscle weakness Causes GAA gene mutation. Diagnosis Enzyme activity, genetic testing. Treatment Enzyme replacement therapy. Which Clinic Should You Go To? Metabolism Clinic What to Do in an Emergency? In case of respiratory failure, 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":"Pompe Disease - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Pompe disease is a lysosomal storage disease characterized by progressive myopathy and cardiomyopathy resulting from a deficiency of the acid alpha-glucosidase enzyme."},"footnotes":""},"class_list":["post-21250","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21250","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\/21250\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21250"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}