{"id":21252,"date":"2025-11-17T01:45:43","date_gmt":"2025-11-16T22:45:43","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/glicogen-depo-2\/"},"modified":"2025-11-17T01:45:43","modified_gmt":"2025-11-16T22:45:43","slug":"glicogen-depo-2","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/glicogen-depo-2\/","title":{"rendered":"Glycogen Storage Disease Type II (Pompe)"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Glycogen storage disease type II is a lysosomal storage disease characterized by acid alpha-glucosidase enzyme deficiency and characterized by myopathy and cardiomyopathy.<\/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 Glycogen storage disease type II is a lysosomal storage disease characterized by acid alpha-glucosidase enzyme deficiency, resulting in myopathy and cardiomyopathy. 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 [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Glycogen Storage Disease Type II (Pompe) - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Glycogen storage disease type II is a lysosomal storage disease characterized by acid alpha-glucosidase enzyme deficiency, resulting in myopathy and cardiomyopathy."},"footnotes":""},"class_list":["post-21252","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21252","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\/21252\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21252"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}