{"id":21254,"date":"2025-11-17T01:45:43","date_gmt":"2025-11-16T22:45:43","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/andersen\/"},"modified":"2025-11-17T01:45:43","modified_gmt":"2025-11-16T22:45:43","slug":"andersen","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/andersen\/","title":{"rendered":"Glycogen Storage Disease Type IV (Andersen)"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Glycogen storage disease type IV is a rare metabolic disease characterized by branching enzyme deficiency, progressive liver cirrhosis, and neuromuscular involvement.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Hepatomegaly<\/li>\n<li>Progressive cirrhosis<\/li>\n<li>Hypotonia<\/li>\n<li>Developmental delay<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>GBE1 gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Liver biopsy, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Liver transplantation.<\/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 liver 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 IV is a rare metabolic disease characterized by branching enzyme deficiency, progressive liver cirrhosis, and neuromuscular involvement. Symptoms Hepatomegaly Progressive cirrhosis Hypotonia Growth retardation Causes GBE1 gene mutation. Diagnosis Liver biopsy, genetic testing. Treatment Liver transplant. Which Clinic Should You Go To? Metabolism Clinic What to Do in an Emergency? In case of liver failure, emergency [\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 IV (Andersen) - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Glycogen storage disease type IV is a rare metabolic disorder characterized by branching enzyme deficiency, progressive liver cirrhosis, and neuromuscular involvement."},"footnotes":""},"class_list":["post-21254","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21254","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\/21254\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21254"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}